Autosomal Recessive Disease

Disease ID: disease_node_13241

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Subclassof	DOID_0050739
Data Source	DOID
Doid Label	autosomal recessive disease
Doid Description	An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop.
Disease Node Id	disease_node_13241
Doid Id	DOID_0050737
Label	Autosomal Recessive Disease

Incoming r'ship SUBCLASS_OF to/from Anauxetic Dysplasia 3(ID:disease_node_15670) (Disease)
Incoming r'ship SUBCLASS_OF to/from Xeroderma Pigmentosum(ID:disease_node_8034) (Disease)
Incoming r'ship SUBCLASS_OF to/from Xanthinuria(ID:disease_node_17500) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zaki Syndrome(ID:disease_node_20312) (Disease)
Incoming r'ship SUBCLASS_OF to/from Yoon-Bellen Neurodevelopmental Syndrome(ID:disease_node_20313) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zellweger Syndrome(ID:disease_node_8124) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 2(ID:disease_node_14350) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tetraamelia Syndrome 2(ID:disease_node_20229) (Disease)
Incoming r'ship SUBCLASS_OF to/from Treacher Collins Syndrome 2(ID:disease_node_19964) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 10(ID:disease_node_19901) (Disease)
Incoming r'ship SUBCLASS_OF to/from Teratozoospermia(ID:disease_node_229) (Disease)
Incoming r'ship SUBCLASS_OF to/from Transient Infantile Liver Failure(ID:disease_node_20515) (Disease)
Incoming r'ship SUBCLASS_OF to/from Troyer Syndrome(ID:disease_node_16680) (Disease)
Incoming r'ship SUBCLASS_OF to/from Thalassemia(ID:disease_node_7352) (Disease)
Incoming r'ship SUBCLASS_OF to/from Treacher Collins Syndrome 3(ID:disease_node_19963) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ullrich Congenital Muscular Dystrophy(ID:disease_node_17423) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 9(ID:disease_node_19902) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 13(ID:disease_node_19898) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 8(ID:disease_node_19903) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wiedemann-Rautenstrauch Syndrome(ID:disease_node_19960) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 7(ID:disease_node_19904) (Disease)
Incoming r'ship SUBCLASS_OF to/from Stress-Induced Childhood-Onset Neurodegeneration With Variable Ataxia And Seizures(ID:disease_node_16102) (Disease)
Incoming r'ship SUBCLASS_OF to/from Whim Syndrome 2(ID:disease_node_20461) (Disease)
Incoming r'ship SUBCLASS_OF to/from Walker-Warburg Syndrome(ID:disease_node_12527) (Disease)
Incoming r'ship SUBCLASS_OF to/from Warsaw Breakage Syndrome(ID:disease_node_20331) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vitamin D-Dependent Rickets Type 1A(ID:disease_node_15716) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vitamin D-Dependent Rickets Type 2A(ID:disease_node_15718) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tango2-Related Metabolic Encephalopathy And Arrythmias(ID:disease_node_20276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Werner Syndrome(ID:disease_node_7969) (Disease)
Incoming r'ship SUBCLASS_OF to/from Triple-A Syndrome(ID:disease_node_20363) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wolfram Syndrome 1(ID:disease_node_20160) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 12(ID:disease_node_19899) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 17(ID:disease_node_14348) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 11(ID:disease_node_19900) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vitamin D-Dependent Rickets Type 1B(ID:disease_node_15715) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tetraamelia Syndrome 1(ID:disease_node_20230) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 6(ID:disease_node_19905) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 67(ID:disease_node_15154) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 15(ID:disease_node_15231) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 28(ID:disease_node_15815) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 60(ID:disease_node_15141) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 47(ID:disease_node_15162) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rnaset2-Deficient Cystic Leukoencephalopathy(ID:disease_node_19918) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 70(ID:disease_node_15212) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 55(ID:disease_node_15148) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 66(ID:disease_node_15155) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocostal Dysostosis 4(ID:disease_node_15611) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 14 With Polydactyly(ID:disease_node_15724) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 39(ID:disease_node_15169) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 45(ID:disease_node_15164) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 77(ID:disease_node_15823) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinal Dystrophy With Leukodystrophy(ID:disease_node_17503) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 75(ID:disease_node_15207) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 19 With Or Without Polydactyly(ID:disease_node_15735) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schindler Disease(ID:disease_node_20482) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 61(ID:disease_node_15146) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 9 With Or Without Polydactyly(ID:disease_node_15723) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 69(ID:disease_node_15833) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 16(ID:disease_node_15160) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 24(ID:disease_node_15166) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 26(ID:disease_node_15157) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 18 With Polydactyly(ID:disease_node_15736) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 35(ID:disease_node_15179) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 82(ID:disease_node_15200) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 85(ID:disease_node_15799) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 41(ID:disease_node_15181) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 83(ID:disease_node_15199) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 58(ID:disease_node_15144) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 8 With Or Without Polydactyly(ID:disease_node_15726) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 20(ID:disease_node_15216) (Disease)
Incoming r'ship SUBCLASS_OF to/from Silverman-Handmaker Type Dyssegmental Dysplasia(ID:disease_node_15648) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa With Or Without Situs Inversus(ID:disease_node_15828) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 76(ID:disease_node_15206) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 71(ID:disease_node_15211) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sitosterolemia 2(ID:disease_node_20478) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 57(ID:disease_node_15147) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocostal Dysostosis 3(ID:disease_node_15613) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 81(ID:disease_node_15824) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 53(ID:disease_node_15225) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 86(ID:disease_node_15197) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 51(ID:disease_node_15134) (Disease)
Incoming r'ship SUBCLASS_OF to/from Seckel Syndrome(ID:disease_node_20368) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sotos Syndrome 3(ID:disease_node_15600) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 8(ID:disease_node_16063) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 90(ID:disease_node_15795) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 78(ID:disease_node_15204) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 92(ID:disease_node_15191) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 68(ID:disease_node_15809) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 30(ID:disease_node_15180) (Disease)
Incoming r'ship SUBCLASS_OF to/from Restrictive Dermopathy 1(ID:disease_node_20573) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short Stature, Hearing Loss, Retinitis Pigmentosa, And Distinctive Facies(ID:disease_node_20347) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepimetaphyseal Dysplasia, Sponastrime Type(ID:disease_node_15663) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 27(ID:disease_node_15167) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 37(ID:disease_node_15168) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 6 With Or Without Polydactyly(ID:disease_node_15728) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 50(ID:disease_node_15839) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 38(ID:disease_node_15814) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 63(ID:disease_node_15140) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 59(ID:disease_node_15139) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 56(ID:disease_node_15811) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sclerosteosis 1(ID:disease_node_13722) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 49(ID:disease_node_15136) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 52(ID:disease_node_15137) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 46(ID:disease_node_15163) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 73(ID:disease_node_15209) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sideroblastic Anemia With B-Cell Immunodeficiency, Periodic Fevers, And Developmental Delay(ID:disease_node_15247) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 79(ID:disease_node_15203) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 44(ID:disease_node_15138) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 69(ID:disease_node_15213) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 28(ID:disease_node_15177) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spinal Muscular Atrophies Of Childhood(ID:disease_node_7964) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia, Sensorineural Hearing Loss, Intellectual Developmental Disorder, And Leber Congenital Amaurosis(ID:disease_node_20227) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 25(ID:disease_node_15173) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 91(ID:disease_node_15192) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocostal Dysostosis 1(ID:disease_node_15610) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 85(ID:disease_node_15153) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 21(ID:disease_node_15159) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sclerosteosis 2(ID:disease_node_13721) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sost-Related Sclerosing Bone Dysplasia(ID:disease_node_13720) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sideroblastic Anemia 5(ID:disease_node_15254) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 31(ID:disease_node_15158) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia 6(ID:disease_node_18058) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 29(ID:disease_node_15165) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 72(ID:disease_node_15210) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 74(ID:disease_node_15208) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 4(ID:disease_node_16067) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia Kondo-Fu Type(ID:disease_node_15693) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 64(ID:disease_node_15143) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 7 With Or Without Polydactyly(ID:disease_node_15730) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 88(ID:disease_node_15195) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 45(ID:disease_node_15835) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 93(ID:disease_node_15190) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 14(ID:disease_node_15224) (Disease)
Incoming r'ship SUBCLASS_OF to/from Recessive Dystrophic Epidermolysis Bullosa(ID:disease_node_14232) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 22(ID:disease_node_15228) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 50(ID:disease_node_15135) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 18(ID:disease_node_15217) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schinzel Type Phocomelia(ID:disease_node_20232) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 40(ID:disease_node_15808) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sandestig-Stefanova Syndrome(ID:disease_node_20269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 89(ID:disease_node_15194) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 65(ID:disease_node_15142) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 72(ID:disease_node_15840) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 57(ID:disease_node_15834) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 94(ID:disease_node_15189) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 17(ID:disease_node_15230) (Disease)
Incoming r'ship SUBCLASS_OF to/from Split Hand-Foot Malformation 1 With Sensorineural Hearing Loss(ID:disease_node_15708) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 34(ID:disease_node_15182) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 9(ID:disease_node_15152) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 48(ID:disease_node_15161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 81(ID:disease_node_15201) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sjogren-Larsson Syndrome(ID:disease_node_8580) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 84(ID:disease_node_15198) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 80(ID:disease_node_15202) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short Stature, Facial Dysmorphism, And Skeletal Anomalies With Or Without Cardiac Anomalies 2(ID:disease_node_20223) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 68(ID:disease_node_15214) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocostal Dysostosis 2(ID:disease_node_15612) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 77(ID:disease_node_15205) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 5(ID:disease_node_16066) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 42(ID:disease_node_15171) (Disease)
Incoming r'ship SUBCLASS_OF to/from Salt And Pepper Syndrome(ID:disease_node_20352) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia 3(ID:disease_node_18059) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 59(ID:disease_node_15822) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 38(ID:disease_node_15174) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 88(ID:disease_node_15797) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylometaphyseal Dysplasia With Corneal Dystrophy(ID:disease_node_15644) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 71(ID:disease_node_15817) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schwartz-Jampel Syndrome 1(ID:disease_node_20261) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 54(ID:disease_node_15150) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 62(ID:disease_node_15805) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 90(ID:disease_node_15193) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Quadriplegic Cerebral Palsy 3(ID:disease_node_20558) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 13(ID:disease_node_15221) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylometaphyseal Dysplasia Megarbane-Dagher-Melike Type(ID:disease_node_15643) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 73(ID:disease_node_15802) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 40(ID:disease_node_15175) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 75(ID:disease_node_15819) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 19(ID:disease_node_15233) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 74(ID:disease_node_15836) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepimetaphyseal Dysplasia With Joint Laxity Type 3(ID:disease_node_15664) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 33(ID:disease_node_15178) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 3(ID:disease_node_16068) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rolandic Epilepsy-Paroxysmal Exercise-Induced Dystonia-Writer'S Cramp Syndrome(ID:disease_node_16305) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 11 With Or Without Polydactyly(ID:disease_node_15725) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ruijs-Aalfs Syndrome(ID:disease_node_20253) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 84(ID:disease_node_15800) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 56(ID:disease_node_15149) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 43(ID:disease_node_15176) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia 5(ID:disease_node_18060) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 10 With Or Without Polydactyly(ID:disease_node_15729) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 62(ID:disease_node_15145) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ritscher-Schinzel Syndrome 1(ID:disease_node_19130) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocarpotarsal Synostosis Syndrome(ID:disease_node_15710) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 87(ID:disease_node_15196) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia 7(ID:disease_node_18055) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocostal Dysostosis 6(ID:disease_node_15614) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia 4(ID:disease_node_18056) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 13 With Or Without Polydactyly(ID:disease_node_15727) (Disease)
Incoming r'ship SUBCLASS_OF to/from Right Atrial Isomerism(ID:disease_node_19910) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepimetaphyseal Dysplasia With Joint Laxity Type 1(ID:disease_node_15666) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 2(ID:disease_node_16069) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 95(ID:disease_node_15188) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 23(ID:disease_node_15222) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Autosomal Recessive Microcephaly(ID:disease_node_19277) (Disease)
Incoming r'ship SUBCLASS_OF to/from Photosensitive Trichothiodystrophy 1(ID:disease_node_19259) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 2B(ID:disease_node_17530) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 4B(ID:disease_node_17524) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 14(ID:disease_node_17207) (Disease)
Incoming r'ship SUBCLASS_OF to/from Prolidase Deficiency(ID:disease_node_12268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 41(ID:disease_node_14673) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pharc Syndrome(ID:disease_node_20309) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pancreatic Agenesis 1(ID:disease_node_14479) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 10(ID:disease_node_17064) (Disease)
Incoming r'ship SUBCLASS_OF to/from Preaxial Polydactyly I(ID:disease_node_20137) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 7B(ID:disease_node_17521) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteasome-Associated Autoinflammatory Syndrome 3(ID:disease_node_15596) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 2(ID:disease_node_16133) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 20(ID:disease_node_16126) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 18(ID:disease_node_17203) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 9(ID:disease_node_16296) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 15(ID:disease_node_16130) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pseudoxanthoma Elasticum(ID:disease_node_6399) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 38(ID:disease_node_14679) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 15(ID:disease_node_16109) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 2E(ID:disease_node_16106) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pulmonary Venoocclusive Disease 2(ID:disease_node_13240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Familial Intrahepatic Cholestasis 5(ID:disease_node_17767) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 18(ID:disease_node_17059) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 1D(ID:disease_node_16115) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 19(ID:disease_node_17222) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 12(ID:disease_node_17209) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 1B(ID:disease_node_16116) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 6B(ID:disease_node_17522) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pantothenate Kinase-Associated Neurodegeneration(ID:disease_node_3648) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 1C(ID:disease_node_16112) (Disease)
Incoming r'ship SUBCLASS_OF to/from Plack Syndrome(ID:disease_node_20583) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 15(ID:disease_node_17206) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 11(ID:disease_node_17055) (Disease)
Incoming r'ship SUBCLASS_OF to/from Polycystic Kidney, Autosomal Recessive(ID:disease_node_9012) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 13(ID:disease_node_17208) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Leukoencephalopathy With Ovarian Failure(ID:disease_node_19922) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 8(ID:disease_node_16295) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pitt-Hopkins-Like Syndrome 2(ID:disease_node_16362) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pancreatic Agenesis 2(ID:disease_node_14478) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 45(ID:disease_node_14674) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 7(ID:disease_node_16131) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paget'S Disease Of Bone 5(ID:disease_node_13716) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pseudohypoaldosteronism(ID:disease_node_6376) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 19A(ID:disease_node_16129) (Disease)
Incoming r'ship SUBCLASS_OF to/from Prune Belly Syndrome(ID:disease_node_6366) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteosome-Associated Autoinflammatory Syndrome 5(ID:disease_node_15595) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 14(ID:disease_node_16110) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 2F(ID:disease_node_16105) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Familial Intrahepatic Cholestasis 4(ID:disease_node_17768) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 13(ID:disease_node_16104) (Disease)
Incoming r'ship SUBCLASS_OF to/from Palmoplantar Keratoderma And Woolly Hair(ID:disease_node_19361) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 10(ID:disease_node_16299) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 1B(ID:disease_node_17527) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pain Insensitivity, Congenital(ID:disease_node_1169) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteosome-Associated Autoinflammatory Syndrome 4(ID:disease_node_15597) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 6(ID:disease_node_16132) (Disease)
Incoming r'ship SUBCLASS_OF to/from Permanent Neonatal Diabetes Mellitus(ID:disease_node_17245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Photosensitive Trichothiodystrophy 3(ID:disease_node_19260) (Disease)
Incoming r'ship SUBCLASS_OF to/from Papillon-Lefevre Disease(ID:disease_node_5863) (Disease)
Incoming r'ship SUBCLASS_OF to/from Photosensitive Trichothiodystrophy 2(ID:disease_node_19261) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 5B(ID:disease_node_17523) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 11(ID:disease_node_16111) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 8(ID:disease_node_17213) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 1B(ID:disease_node_16294) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 40(ID:disease_node_14678) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 42(ID:disease_node_14676) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 1E(ID:disease_node_16114) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 2D(ID:disease_node_16107) (Disease)
Incoming r'ship SUBCLASS_OF to/from Perrault Syndrome(ID:disease_node_20349) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 11B(ID:disease_node_17518) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pycnodysostosis(ID:disease_node_12600) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 3B(ID:disease_node_17526) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 1F(ID:disease_node_16113) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 6(ID:disease_node_16297) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 19(ID:disease_node_17062) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 1A(ID:disease_node_16293) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 12(ID:disease_node_16108) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 16(ID:disease_node_16103) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 44(ID:disease_node_14680) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 9(ID:disease_node_17212) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 8B(ID:disease_node_17520) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Coenzyme Q10 Deficiency 9(ID:disease_node_17015) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 10(ID:disease_node_17211) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 25(ID:disease_node_16125) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pontocerebellar Hypoplasia Type 1A(ID:disease_node_16117) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 14B(ID:disease_node_17525) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 39(ID:disease_node_14677) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 10B(ID:disease_node_17517) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 8(ID:disease_node_17061) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 23(ID:disease_node_16127) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 9B(ID:disease_node_17519) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pseudo-Torch Syndrome 1(ID:disease_node_20356) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Pseudorheumatoid Arthropathy Of Childhood(ID:disease_node_15649) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteasome-Associated Autoinflammatory Syndrome 1(ID:disease_node_15599) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 6(ID:disease_node_17012) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 4(ID:disease_node_14942) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mosaic Variegated Aneuploidy Syndrome 2(ID:disease_node_20290) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 9(ID:disease_node_18447) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonphotosensitive Trichothiodystrophy 6(ID:disease_node_19257) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodevelopmental Disorder With Midbrain And Hindbrain Malformations(ID:disease_node_16366) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 3(ID:disease_node_14943) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 18(ID:disease_node_15634) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 5(ID:disease_node_14941) (Disease)
Incoming r'ship SUBCLASS_OF to/from Miyoshi Muscular Dystrophy 1(ID:disease_node_18920) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodegeneration With Brain Iron Accumulation 2A(ID:disease_node_16095) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 17(ID:disease_node_17001) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 19(ID:disease_node_16994) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 7(ID:disease_node_15964) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 3(ID:disease_node_15954) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oguchi Disease-1(ID:disease_node_20055) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 12(ID:disease_node_15620) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 21(ID:disease_node_19070) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodevelopmental Disorder With Cardiomyopathy, Spasticity, And Brain Abnormalities(ID:disease_node_16833) (Disease)
Incoming r'ship SUBCLASS_OF to/from Otulipenia(ID:disease_node_18165) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 16(ID:disease_node_19088) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Xx(ID:disease_node_19250) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 3(ID:disease_node_18452) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodegeneration With Brain Iron Accumulation 4(ID:disease_node_16093) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type C8(ID:disease_node_17395) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 25(ID:disease_node_17011) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonphotosensitive Trichothiodystrophy 8(ID:disease_node_19263) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B4(ID:disease_node_17399) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 10(ID:disease_node_15960) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 12(ID:disease_node_19079) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Mitochondrial Dysfunctions Syndrome 6(ID:disease_node_16817) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 31(ID:disease_node_17007) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oguchi Disease-2(ID:disease_node_20054) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 10(ID:disease_node_19080) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 6B(ID:disease_node_15955) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mucopolysaccharidosis Iii(ID:disease_node_5264) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 13(ID:disease_node_15626) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 2(ID:disease_node_16996) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodegeneration With Brain Iron Accumulation 6(ID:disease_node_16091) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonphotosensitive Trichothiodystrophy 7(ID:disease_node_19258) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 17(ID:disease_node_15630) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neonatal Diabetes Mellitus With Congenital Hypothyroidism(ID:disease_node_17246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Disc Anomalies With Retinal And/Or Macular Dystrophy(ID:disease_node_16613) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 10(ID:disease_node_17004) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Xvi(ID:disease_node_19249) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 6A(ID:disease_node_15956) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 6(ID:disease_node_14940) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 1(ID:disease_node_18984) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 10(ID:disease_node_18974) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 9(ID:disease_node_15952) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Sulfatase Deficiency Disease(ID:disease_node_11561) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B5(ID:disease_node_17405) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mucopolysaccharidosis I(ID:disease_node_4775) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 35(ID:disease_node_17013) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 13(ID:disease_node_15958) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 9(ID:disease_node_19075) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 34(ID:disease_node_16988) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 28(ID:disease_node_16984) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 21(ID:disease_node_16991) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuroacanthocytosis(ID:disease_node_11953) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B2(ID:disease_node_17398) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 33(ID:disease_node_16982) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mosaic Variegated Aneuploidy Syndrome 3(ID:disease_node_20289) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3(ID:disease_node_16971) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Ii(ID:disease_node_19253) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Mitochondrial Dysfunctions Syndrome 4(ID:disease_node_16812) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 11(ID:disease_node_15617) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 6(ID:disease_node_19082) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 10(ID:disease_node_14945) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 22(ID:disease_node_17009) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 9(ID:disease_node_18938) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrogenic Diabetes Insipidus Type 2(ID:disease_node_19685) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 3(ID:disease_node_18932) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 13(ID:disease_node_19085) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 15(ID:disease_node_15621) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neonatal-Onset Type Ii Citrullinemia(ID:disease_node_13243) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 3(ID:disease_node_19084) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mucolipidosis Iii Alpha/Beta(ID:disease_node_20505) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 8 Northern Epilepsy Variant(ID:disease_node_15961) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 9(ID:disease_node_15619) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type C12(ID:disease_node_17396) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Atrophy 9(ID:disease_node_17289) (Disease)
Incoming r'ship SUBCLASS_OF to/from N-Acetylglutamate Synthase Deficiency(ID:disease_node_20554) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 26(ID:disease_node_16993) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 8(ID:disease_node_19077) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 4(ID:disease_node_16997) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myoclonic Epilepsies, Progressive(ID:disease_node_10191) (Disease)
Incoming r'ship SUBCLASS_OF to/from Netherton Syndrome(ID:disease_node_12300;disease_node_20576) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 20(ID:disease_node_15633) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Epiphyseal Dysplasia 7(ID:disease_node_15640) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephronophthisis(ID:disease_node_19859) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 1(ID:disease_node_19076) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Mitochondrial Dysfunctions Syndrome 1(ID:disease_node_16815) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 1(ID:disease_node_17005) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1(ID:disease_node_16973) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 11(ID:disease_node_16990) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 11(ID:disease_node_15953) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 2(ID:disease_node_19087) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 15(ID:disease_node_19089) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 8(ID:disease_node_16998) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 8(ID:disease_node_15631) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 18(ID:disease_node_17008) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 19(ID:disease_node_19072) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia And Hydranencephaly(ID:disease_node_20311) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Xviii(ID:disease_node_19251) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 1(ID:disease_node_14944) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 23(ID:disease_node_19071) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nagashima-Type Palmoplantar Keratosis(ID:disease_node_19360) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 5(ID:disease_node_17010) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 4(ID:disease_node_16970) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 1(ID:disease_node_15965) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B3(ID:disease_node_17400) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 7(ID:disease_node_19078) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 9(ID:disease_node_17006) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 5(ID:disease_node_19086) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 10(ID:disease_node_18936) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B1(ID:disease_node_17403) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mulibrey Nanism(ID:disease_node_11448) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Atrophy 11(ID:disease_node_17292) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nestor-Guillermo Progeria Syndrome(ID:disease_node_19959) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mosaic Variegated Aneuploidy Syndrome 1(ID:disease_node_20291) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B6(ID:disease_node_17404) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mucopolysaccharidosis Iv(ID:disease_node_5269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Xix(ID:disease_node_19252) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 8(ID:disease_node_18978) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 9(ID:disease_node_14946) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Xvii(ID:disease_node_19248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 8(ID:disease_node_15962) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 27(ID:disease_node_16989) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Mitochondrial Dysfunctions Syndrome 5(ID:disease_node_16816) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodegeneration With Brain Iron Accumulation 2B(ID:disease_node_16094) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonphotosensitive Trichothiodystrophy 9(ID:disease_node_19262) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Mitochondrial Dysfunctions Syndrome 3(ID:disease_node_16813) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Mitochondrial Dysfunctions Syndrome 2(ID:disease_node_16814) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 32(ID:disease_node_16999) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B14(ID:disease_node_17401) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 29(ID:disease_node_16995) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myopathy With Extrapyramidal Signs(ID:disease_node_18925) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy-Dystroglycanopathy Type B15(ID:disease_node_17402) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteosclerotic Metaphyseal Dysplasia(ID:disease_node_15676) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 3(ID:disease_node_16986) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 24(ID:disease_node_17000) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 11(ID:disease_node_19081) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 18(ID:disease_node_19073) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 10(ID:disease_node_15622) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 21(ID:disease_node_15616) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 15(ID:disease_node_17002) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 11(ID:disease_node_18933) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 7(ID:disease_node_16987) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myopathy, Central Core(ID:disease_node_10605) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 14(ID:disease_node_19090) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 7(ID:disease_node_18979) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 13(ID:disease_node_17003) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oxoglutarate Dehydrogenase Deficiency(ID:disease_node_20524) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 5B(ID:disease_node_18935) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 7(ID:disease_node_14939) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndrome Xiv(ID:disease_node_19254) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 16(ID:disease_node_16983) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nezelof Syndrome(ID:disease_node_20003) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mosaic Variegated Aneuploidy Syndrome 4(ID:disease_node_20293) (Disease)
Incoming r'ship SUBCLASS_OF to/from Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive(ID:disease_node_15674) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 23(ID:disease_node_16992) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nijmegen Breakage Syndrome(ID:disease_node_11410) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofacial Cleft 14(ID:disease_node_14027) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 8(ID:disease_node_18937) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonphotosensitive Trichothiodystrophy 4(ID:disease_node_19256) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 22(ID:disease_node_19069) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neonatal Lethal Pontocerebellar Hypoplasia, Hypotonia, And Respiratory Insufficiency Syndrome(ID:disease_node_20267) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 17(ID:disease_node_19074) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 14(ID:disease_node_16985) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 2(ID:disease_node_15959) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 5(ID:disease_node_15957) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 5(ID:disease_node_19272) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 5(ID:disease_node_19107) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 20(ID:disease_node_16781) (Disease)
Incoming r'ship SUBCLASS_OF to/from Larsen-Like Syndrome B3Gat3 Type(ID:disease_node_20330) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 7(ID:disease_node_16794) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 7(ID:disease_node_20118) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 1(ID:disease_node_19113) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 22(ID:disease_node_16779) (Disease)
Incoming r'ship SUBCLASS_OF to/from Keratosis Pilaris Atrophicans(ID:disease_node_19983) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly, Seizures, And Developmental Delay(ID:disease_node_16207) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 12(ID:disease_node_16771) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mahvash Disease(ID:disease_node_14475) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lymphoproliferative Syndrome 2(ID:disease_node_20434) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly And Chorioretinopathy 3(ID:disease_node_20314) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 16(ID:disease_node_19111) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 8(ID:disease_node_16774) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 13(ID:disease_node_16786) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 4B(ID:disease_node_16797) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 4(ID:disease_node_20120) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 19(ID:disease_node_16827) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 1(ID:disease_node_20123) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 2(ID:disease_node_16789) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lethal Congenital Contracture Syndrome(ID:disease_node_20327) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lafora Disease(ID:disease_node_10193) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 9(ID:disease_node_19110) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 15(ID:disease_node_16819) (Disease)
Incoming r'ship SUBCLASS_OF to/from Methemoglobinemia And Ambiguous Genitalia(ID:disease_node_17165) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 18(ID:disease_node_16828) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 13(ID:disease_node_16822) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 1(ID:disease_node_16778) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mismatch Repair Cancer Syndrome(ID:disease_node_20231) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 3(ID:disease_node_16777) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 6(ID:disease_node_16788) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 23(ID:disease_node_16784) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 2(ID:disease_node_19109) (Disease)
Incoming r'ship SUBCLASS_OF to/from Laron Syndrome(ID:disease_node_11271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 11(ID:disease_node_16772) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly And Chorioretinopathy 1(ID:disease_node_20317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 12B(ID:disease_node_16821) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meckel Syndrome 13(ID:disease_node_14684) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 15(ID:disease_node_16769) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 11(ID:disease_node_16824) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 10(ID:disease_node_16773) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 14(ID:disease_node_16770) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 21(ID:disease_node_16780) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 7 With Cerebellar Hypoplasia(ID:disease_node_19271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leukocyte-Adhesion Deficiency Syndrome(ID:disease_node_9688) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 9(ID:disease_node_16787) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Feil Syndrome 2(ID:disease_node_17382) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 4B(ID:disease_node_16825) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 17(ID:disease_node_16829) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 15(ID:disease_node_19108) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Pyruvate Carrier Deficiency(ID:disease_node_16811) (Disease)
Incoming r'ship SUBCLASS_OF to/from Megalencephalic Leukoencephalopathy With Subcortical Cysts 2A(ID:disease_node_19920) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 19(ID:disease_node_16782) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 16(ID:disease_node_16768) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lymphoproliferative Syndrome 1(ID:disease_node_20435) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 17(ID:disease_node_16767) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 2(ID:disease_node_20122) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lysosomal Acid Lipase Deficiency(ID:disease_node_20502) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 7(ID:disease_node_16775) (Disease)
Incoming r'ship SUBCLASS_OF to/from Megaconial Type Congenital Muscular Dystrophy(ID:disease_node_17421) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 8(ID:disease_node_19112) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 8(ID:disease_node_19270) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Feil Syndrome 4(ID:disease_node_17380) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly, Short Stature, And Limb Abnormalities(ID:disease_node_15650) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly And Chorioretinopathy 2(ID:disease_node_20315) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 4(ID:disease_node_16776) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 20(ID:disease_node_16826) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 3(ID:disease_node_20121) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency(ID:disease_node_16834) (Disease)
Incoming r'ship SUBCLASS_OF to/from Laurence-Moon Syndrome(ID:disease_node_4594) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microphthalmia With Limb Anomalies(ID:disease_node_20326) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 4(ID:disease_node_19269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Late-Adult Onset Retinitis Pigmentosa(ID:disease_node_15826) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 16(ID:disease_node_16831) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex Iv Deficiency Nuclear Type 18(ID:disease_node_16783) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 5(ID:disease_node_20119) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 17(ID:disease_node_19115) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 8(ID:disease_node_20124) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 16B(ID:disease_node_16830) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 5(ID:disease_node_16795) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mandibuloacral Dysplasia Type B Lipodystrophy(ID:disease_node_15712) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 6(ID:disease_node_19268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Marinesco-Sjogren Syndrome(ID:disease_node_20300) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leukoencephalopathy With Vanishing White Matter(ID:disease_node_19949) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 15(ID:disease_node_19935) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 32(ID:disease_node_16626) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperphosphatemic Familial Tumoral Calcinosis(ID:disease_node_17442) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 7(ID:disease_node_20004) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 27(ID:disease_node_16630) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency With Hyper-Igm Type 2(ID:disease_node_17343) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spherocytosis Type 5(ID:disease_node_15277) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyaline Fibromatosis Syndrome(ID:disease_node_12420) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 11(ID:disease_node_19943) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 1(ID:disease_node_16607) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 7(ID:disease_node_14203) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 44(ID:disease_node_20444) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 11(ID:disease_node_16644) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 11A(ID:disease_node_13319) (Disease)
Incoming r'ship SUBCLASS_OF to/from Junctional Epidermolysis Bullosa With Pyloric Atresia(ID:disease_node_14239) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 17(ID:disease_node_20006) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 4(ID:disease_node_19946) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 64(ID:disease_node_13338) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 9(ID:disease_node_19944) (Disease)
Incoming r'ship SUBCLASS_OF to/from Homocystinuria-Megaloblastic Anemia Cble Type(ID:disease_node_20520) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 6(ID:disease_node_16612) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 15(ID:disease_node_14209) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Arterial And Articular Multiple Calcification Syndrome(ID:disease_node_20247) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 21(ID:disease_node_19926) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 2B(ID:disease_node_19418) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hemoglobin Sc Disease(ID:disease_node_3807) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 22(ID:disease_node_13321) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 9B(ID:disease_node_16646) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 26(ID:disease_node_16631) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 56(ID:disease_node_16663) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 13 With Or Without Anosmia(ID:disease_node_17197) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 56(ID:disease_node_13313) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 26(ID:disease_node_13317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperekplexia 4(ID:disease_node_20162) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 25(ID:disease_node_16632) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 70(ID:disease_node_16679) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 79B(ID:disease_node_16622) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 45(ID:disease_node_20455) (Disease)
Incoming r'ship SUBCLASS_OF to/from Junctional Epidermolysis Bullosa Non-Herlitz Type(ID:disease_node_14237) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 89(ID:disease_node_16675) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile Liver Failure Syndrome 1(ID:disease_node_20282) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 23(ID:disease_node_13300) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 40(ID:disease_node_13301) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile Parkinsonism-Dystonia 2(ID:disease_node_16711) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 14(ID:disease_node_19925) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 5(ID:disease_node_16610) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 45(ID:disease_node_16682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperekplexia(ID:disease_node_150) (Disease)
Incoming r'ship SUBCLASS_OF to/from Interstitial Lung Disease 1(ID:disease_node_14636) (Disease)
Incoming r'ship SUBCLASS_OF to/from Homocystinuria-Megaloblastic Anemia Cblg Type(ID:disease_node_20519) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyper Ige Recurrent Infection Syndrome 3(ID:disease_node_17340) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 3(ID:disease_node_19945) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 29(ID:disease_node_20447) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 8(ID:disease_node_14202) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 18(ID:disease_node_16637) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inflammatory Bowel Disease 25(ID:disease_node_14188) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 5A(ID:disease_node_16661) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 18(ID:disease_node_19934) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 24(ID:disease_node_16633) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 2(ID:disease_node_16608) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 47(ID:disease_node_16672) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperprolinemia Type 1(ID:disease_node_20530) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 62(ID:disease_node_17346) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inflammatory Bowel Disease 28(ID:disease_node_14189) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hmg-Coa Synthase 2 Deficiency(ID:disease_node_20538) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 53(ID:disease_node_13307) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 6(ID:disease_node_14204) (Disease)
Incoming r'ship SUBCLASS_OF to/from Histiocytosis-Lymphadenopathy Plus Syndrome(ID:disease_node_20252) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 46(ID:disease_node_16681) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperglycinemia, Nonketotic(ID:disease_node_10126) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 32B(ID:disease_node_13336) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 7(ID:disease_node_16655) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 9(ID:disease_node_14201) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 55(ID:disease_node_16664) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spherocytosis Type 1(ID:disease_node_15281) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 10(ID:disease_node_14200) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 76(ID:disease_node_16650) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 35(ID:disease_node_16693) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 49(ID:disease_node_16670) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 2(ID:disease_node_19948) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathies(ID:disease_node_5589) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 65(ID:disease_node_20443) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 28(ID:disease_node_16629) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 20(ID:disease_node_19924) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 23(ID:disease_node_16634) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyper Ige Recurrent Infection Syndrome 4(ID:disease_node_17339) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 63(ID:disease_node_16657) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory Neuropathy Type 2C(ID:disease_node_19419) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 15(ID:disease_node_16640) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 43(ID:disease_node_16684) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 19(ID:disease_node_13316) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 83(ID:disease_node_16620) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 63(ID:disease_node_20458) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 44(ID:disease_node_16683) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 18 With Or Without Anosmia(ID:disease_node_17194) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 16(ID:disease_node_13305) (Disease)
Incoming r'ship SUBCLASS_OF to/from Iga Deficiency(ID:disease_node_9044) (Disease)
Incoming r'ship SUBCLASS_OF to/from High Myopia-Sensorineural Deafness Syndrome(ID:disease_node_20240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperekplexia 2(ID:disease_node_20163) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 8(ID:disease_node_16606) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 17(ID:disease_node_19929) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 86(ID:disease_node_16624) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 23(ID:disease_node_19936) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 2A(ID:disease_node_19417) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 11 With Or Without Anosmia(ID:disease_node_17199) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 87(ID:disease_node_16677) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 52(ID:disease_node_20009) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spherocytosis Type 3(ID:disease_node_15279) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 12 With Or Without Anosmia(ID:disease_node_17198) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 13(ID:disease_node_19940) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 57(ID:disease_node_20446) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 15B(ID:disease_node_13318) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 31B(ID:disease_node_20448) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 52(ID:disease_node_16667) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Hyperchlorhidrosis(ID:disease_node_20556) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 79(ID:disease_node_20010) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Pyropoikilocytosis(ID:disease_node_15285) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile Cerebral And Cerebellar Atrophy With Postnatal Progressive Microcephaly(ID:disease_node_20557) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 71(ID:disease_node_13341) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 6(ID:disease_node_19424) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 64(ID:disease_node_16656) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 69(ID:disease_node_20457) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 22 With Or Without Anosmia(ID:disease_node_17189) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 66(ID:disease_node_20452) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 72(ID:disease_node_13340) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 85(ID:disease_node_16621) (Disease)
Incoming r'ship SUBCLASS_OF to/from Junctional Epidermolysis Bullosa Herlitz Type(ID:disease_node_14238) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 18(ID:disease_node_20445) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 37(ID:disease_node_13304) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 82(ID:disease_node_16623) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 72A(ID:disease_node_16654) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency With Hyper Igm Type 5(ID:disease_node_17342) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 51(ID:disease_node_16668) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 7 With Or Without Anosmia(ID:disease_node_17192) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 8(ID:disease_node_19423) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 55(ID:disease_node_13344) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 26(ID:disease_node_19930) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 24 Without Anosmia(ID:disease_node_17182) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 53(ID:disease_node_16666) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inflammatory Poikiloderma With Hair Abnormalities And Acral Keratoses(ID:disease_node_20584) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 75(ID:disease_node_16651) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 12(ID:disease_node_13345) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 28(ID:disease_node_20454) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hermanski-Pudlak Syndrome(ID:disease_node_10905) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ichthyosis, Lamellar(ID:disease_node_9185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 57(ID:disease_node_16662) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intellectual Developmental Disorder With Cardiac Arrhythmia(ID:disease_node_20280) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 42(ID:disease_node_20450) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 50(ID:disease_node_16669) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile Cerebellar-Retinal Degeneration(ID:disease_node_16142) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intellectual Developmental Disorder With Short Stature And Behavioral Abnormalities(ID:disease_node_20237) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypervalinemia And Hyperleucine-Isoleucinemia(ID:disease_node_20536) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperlipoproteinemia Type I(ID:disease_node_4796) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 84(ID:disease_node_16619) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 78(ID:disease_node_16618) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 23 With Or Without Anosmia(ID:disease_node_17179) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome(ID:disease_node_20256) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 24(ID:disease_node_13320) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kenny-Caffey Syndrome Type 1(ID:disease_node_15653) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 8 With Or Without Anosmia(ID:disease_node_17196) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 3(ID:disease_node_16605) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 62(ID:disease_node_16658) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 20(ID:disease_node_20449) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency With Hyper Igm Type 3(ID:disease_node_17344) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hengel-Maroofian-Schols Syndrome(ID:disease_node_20320) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 81(ID:disease_node_16617) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 77(ID:disease_node_16649) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 58(ID:disease_node_13312) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 12(ID:disease_node_19939) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 74(ID:disease_node_16652) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 39(ID:disease_node_16689) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 14(ID:disease_node_16641) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperekplexia 3(ID:disease_node_20161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 46(ID:disease_node_13303) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 5(ID:disease_node_19942) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 10(ID:disease_node_19947) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 38(ID:disease_node_20451) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 8(ID:disease_node_19938) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Angioedema Type I(ID:disease_node_19966) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 7(ID:disease_node_19941) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 54(ID:disease_node_16665) (Disease)
Incoming r'ship SUBCLASS_OF to/from Karyomegalic Interstitial Nephritis(ID:disease_node_15774) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 48(ID:disease_node_16671) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 73C With Defective Neutrophil Chemotaxis And Hypogammaglobulinemia(ID:disease_node_13333) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyper Ige Recurrent Infection Syndrome 2(ID:disease_node_17341) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 61(ID:disease_node_16659) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 30(ID:disease_node_20459) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 10 With Or Without Anosmia(ID:disease_node_17181) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 51(ID:disease_node_20453) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fatal Infantile Hypertonic Myofibrillar Myopathy(ID:disease_node_18977) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Akinesia Deformation Sequence Syndrome 3(ID:disease_node_19104) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gitelman Syndrome(ID:disease_node_11740) (Disease)
Incoming r'ship SUBCLASS_OF to/from Growth Hormone Insensitivity Syndrome With Immune Dysregulation 1(ID:disease_node_20294) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Ic(ID:disease_node_20391) (Disease)
Incoming r'ship SUBCLASS_OF to/from Halperin-Birk Syndrome(ID:disease_node_20319) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fazio-Londe Disease(ID:disease_node_18000) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycosuria, Renal(ID:disease_node_3544) (Disease)
Incoming r'ship SUBCLASS_OF to/from Eye Diseases(ID:disease_node_3102) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ghosal Hematodiaphyseal Syndrome(ID:disease_node_20224) (Disease)
Incoming r'ship SUBCLASS_OF to/from Factor X Deficiency(ID:disease_node_3144) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Lipase Maturation Factor 1 Deficiency(ID:disease_node_16846) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group D2(ID:disease_node_15301) (Disease)
Incoming r'ship SUBCLASS_OF to/from Heimler Syndrome 1(ID:disease_node_17529) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gangliosidoses(ID:disease_node_3377) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group E(ID:disease_node_15300) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group W(ID:disease_node_15306) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frontonasal Dysplasia 2(ID:disease_node_20278) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gapo Syndrome(ID:disease_node_20225) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Vii(ID:disease_node_3532) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group A(ID:disease_node_15289) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group O(ID:disease_node_15288) (Disease)
Incoming r'ship SUBCLASS_OF to/from Factor Xii Deficiency(ID:disease_node_3152) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 5(ID:disease_node_16288) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fibrochondrogenesis 2(ID:disease_node_15679) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hemophagocytic Lymphohistiocytosis 3(ID:disease_node_18245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Akinesia Deformation Sequence Syndrome 4(ID:disease_node_19101) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Partial Lipodystrophy Type 6(ID:disease_node_20143) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Isolated Trichomegaly(ID:disease_node_19661) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Partial Lipodystrophy Type 5(ID:disease_node_20144) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis Et Progressiva 1(ID:disease_node_19131) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hemophagocytic Lymphohistiocytosis 1(ID:disease_node_18247) (Disease)
Incoming r'ship SUBCLASS_OF to/from Factor V Deficiency(ID:disease_node_3136) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Ii(ID:disease_node_3516) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis Et Progressiva 4(ID:disease_node_19134) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glutaric Acidemia Type 3(ID:disease_node_17501) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Ia(ID:disease_node_20390) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adenomatous Polyposis 2(ID:disease_node_17034) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Xv(ID:disease_node_20397) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group U(ID:disease_node_15299) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Erythrocytosis 2(ID:disease_node_15335) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hemophagocytic Lymphohistiocytosis 4(ID:disease_node_18244) (Disease)
Incoming r'ship SUBCLASS_OF to/from Heimler Syndrome 2(ID:disease_node_17528) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glucocorticoid Deficiency 1(ID:disease_node_17793) (Disease)
Incoming r'ship SUBCLASS_OF to/from Galactosemias(ID:disease_node_3363) (Disease)
Incoming r'ship SUBCLASS_OF to/from Galloway-Mowat Syndrome 3(ID:disease_node_20286) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Encasement Syndrome(ID:disease_node_20324) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Ib(ID:disease_node_20392) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frontonasal Dysplasia 1(ID:disease_node_20279) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frontonasal Dysplasia 3(ID:disease_node_20277) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gaucher'S Disease Type Iii(ID:disease_node_20493) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 4(ID:disease_node_16859) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adenomatous Polyposis 3(ID:disease_node_17033) (Disease)
Incoming r'ship SUBCLASS_OF to/from Factor Xiii Deficiency(ID:disease_node_3156) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group C(ID:disease_node_15297) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group Q(ID:disease_node_15291) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Gpihbp1 Deficiency(ID:disease_node_16848) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 1(ID:disease_node_16855) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Akinesia Deformation Sequence Syndrome 1(ID:disease_node_19103) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type V(ID:disease_node_3528) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 5(ID:disease_node_13371) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Renotubular Syndrome 2(ID:disease_node_19161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Segmental Glomerulosclerosis 6(ID:disease_node_15778) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fraser Syndrome(ID:disease_node_12538) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adenomatous Polyposis 4(ID:disease_node_17032) (Disease)
Incoming r'ship SUBCLASS_OF to/from Galloway-Mowat Syndrome 1(ID:disease_node_20288) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group T(ID:disease_node_15303) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Iv(ID:disease_node_3526) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group L(ID:disease_node_15302) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Akinesia Deformation Sequence Syndrome 2(ID:disease_node_19102) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group V(ID:disease_node_15304) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Restrictive Cardiomyopathy 6(ID:disease_node_16874) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hepatic Adenoma(ID:disease_node_17780) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hemophagocytic Lymphohistiocytosis 2(ID:disease_node_18246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Galloway-Mowat Syndrome 4(ID:disease_node_20285) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glutatione Synthetase Deficiency With 5-Oxoprolinuria(ID:disease_node_15260) (Disease)
Incoming r'ship SUBCLASS_OF to/from Factor Vii Deficiency(ID:disease_node_3140) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 2(ID:disease_node_16856) (Disease)
Incoming r'ship SUBCLASS_OF to/from Giant Axonal Neuropathy(ID:disease_node_12285) (Disease)
Incoming r'ship SUBCLASS_OF to/from Geleophysic Dysplasia 1(ID:disease_node_15707) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 8(ID:disease_node_16853) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Segmental Glomerulosclerosis 9(ID:disease_node_15775) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Renotubular Syndrome 5(ID:disease_node_19158) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group P(ID:disease_node_15292) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fibrochondrogenesis 1(ID:disease_node_15680) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group D1(ID:disease_node_15295) (Disease)
Incoming r'ship SUBCLASS_OF to/from Foveal Hypoplasia 2(ID:disease_node_20572) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Iii(ID:disease_node_3524) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis Et Progressiva 5(ID:disease_node_19133) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group S(ID:disease_node_15305) (Disease)
Incoming r'ship SUBCLASS_OF to/from Griscelli Syndrome(ID:disease_node_18455) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Vi(ID:disease_node_3530) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group I(ID:disease_node_15293) (Disease)
Incoming r'ship SUBCLASS_OF to/from Harel-Yoon Syndrome(ID:disease_node_20086) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 13(ID:disease_node_18087) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cortisone Reductase Deficiency 1(ID:disease_node_17241) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 6(ID:disease_node_18956) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 61(ID:disease_node_16229) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Musculocontractural Type 1(ID:disease_node_18761) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 107(ID:disease_node_16245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 31B(ID:disease_node_16262) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 105(ID:disease_node_16247) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 29(ID:disease_node_16212) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 13(ID:disease_node_14281) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Classic-Like 2(ID:disease_node_18765) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 48(ID:disease_node_16215) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolysis Bullosa Simplex With Muscular Dystrophy(ID:disease_node_20254) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1C(ID:disease_node_20047) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 18(ID:disease_node_16192) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2B(ID:disease_node_16901) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 19(ID:disease_node_18954) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 22A(ID:disease_node_18951) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 31(ID:disease_node_17272) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 17(ID:disease_node_14283) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1D(ID:disease_node_20046) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 6(ID:disease_node_18082) (Disease)
Incoming r'ship SUBCLASS_OF to/from Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1B(ID:disease_node_19118) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 84(ID:disease_node_16170) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 4(ID:disease_node_18083) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 8(ID:disease_node_14301) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 28(ID:disease_node_16211) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 71(ID:disease_node_16181) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 12(ID:disease_node_16205) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 14(ID:disease_node_18965) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 1B(ID:disease_node_14295) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1G(ID:disease_node_20053) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 2B(ID:disease_node_18949) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermodysplasia Verruciformis(ID:disease_node_2963) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 7(ID:disease_node_14421) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 22B(ID:disease_node_18950) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 38(ID:disease_node_16188) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 22, Juvenile-Onset(ID:disease_node_17265) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 3(ID:disease_node_15267) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 75(ID:disease_node_16177) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 7(ID:disease_node_18081) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 6(ID:disease_node_14286) (Disease)
Incoming r'ship SUBCLASS_OF to/from Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 2(ID:disease_node_20321) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 44(ID:disease_node_16266) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 21(ID:disease_node_16220) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 3B(ID:disease_node_14292) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 35(ID:disease_node_16206) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 9(ID:disease_node_14287) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 110(ID:disease_node_16243) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Myopathy With Anterior Tibial Onset(ID:disease_node_18918) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 53(ID:disease_node_16200) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 22, Adult-Onset(ID:disease_node_17264) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 32(ID:disease_node_17271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 16(ID:disease_node_16214) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 86(ID:disease_node_16169) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2D(ID:disease_node_16922) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 3C(ID:disease_node_14293) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 4A(ID:disease_node_14279) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2G(ID:disease_node_16919) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 19(ID:disease_node_14284) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 25(ID:disease_node_16164) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 89(ID:disease_node_16166) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ellis-Van Creveld Syndrome(ID:disease_node_2761) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniotubular Dysplasia Ikegawa Type(ID:disease_node_19045) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 12(ID:disease_node_14298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 5D(ID:disease_node_15789) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 4(ID:disease_node_15266) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 14(ID:disease_node_18079) (Disease)
Incoming r'ship SUBCLASS_OF to/from Early-Onset Myopathy-Areflexia-Respiratory Distress-Dysphagia Syndrome(ID:disease_node_18939) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 106(ID:disease_node_16246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diphthamide Deficiency Syndrome(ID:disease_node_20531) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 37(ID:disease_node_16228) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cystic Fibrosis(ID:disease_node_2353) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 14(ID:disease_node_14288) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 5(ID:disease_node_18084) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Cardiac Valvular Type(ID:disease_node_18767) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 51(ID:disease_node_16230) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 101(ID:disease_node_16251) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Kyphoscoliotic Type 1(ID:disease_node_18763) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 17(ID:disease_node_18962) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 27(ID:disease_node_17276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Secretory Sodium Diarrhea 8(ID:disease_node_19342) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2A(ID:disease_node_16882) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 9A(ID:disease_node_18945) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 4B(ID:disease_node_14280) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Spondylodysplastic Type 1(ID:disease_node_18759) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1H(ID:disease_node_20048) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 5(ID:disease_node_18947) (Disease)
Incoming r'ship SUBCLASS_OF to/from D-2-Hydroxyglutaric Aciduria 1(ID:disease_node_16047) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 8(ID:disease_node_18080) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 4C(ID:disease_node_14278) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 10B(ID:disease_node_18943) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1E(ID:disease_node_20045) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 21(ID:disease_node_14285) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 50(ID:disease_node_16270) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 5(ID:disease_node_15265) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 18(ID:disease_node_18961) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 88(ID:disease_node_16167) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dopa-Responsive Dystonia(ID:disease_node_14347) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Musculocontractural Type 2(ID:disease_node_18760) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 33(ID:disease_node_17270) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 4(ID:disease_node_14428) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 22(ID:disease_node_14297) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 1(ID:disease_node_14425) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 49(ID:disease_node_16222) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 2C(ID:disease_node_14277) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1B(ID:disease_node_20049) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 11(ID:disease_node_14282) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 80(ID:disease_node_16173) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 15(ID:disease_node_16191) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 11B(ID:disease_node_18094) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 95(ID:disease_node_16256) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 82(ID:disease_node_16187) (Disease)
Incoming r'ship SUBCLASS_OF to/from Donohue Syndrome(ID:disease_node_12263) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 52(ID:disease_node_16209) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 8(ID:disease_node_15264) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 60(ID:disease_node_16231) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 15(ID:disease_node_18086) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cytochrome P450 Oxidoreductase Deficiency(ID:disease_node_16835) (Disease)
Incoming r'ship SUBCLASS_OF to/from Corticosterone Methyloxidase Deficiency 1(ID:disease_node_17791) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2F(ID:disease_node_16920) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Secretory Sodium Diarrhea 3(ID:disease_node_19341) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 5(ID:disease_node_14290) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dna Ligase Iv Deficiency(ID:disease_node_13311) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 15(ID:disease_node_14300) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 10(ID:disease_node_14289) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 9B(ID:disease_node_18944) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Kyphoscoliotic Type 2(ID:disease_node_18762) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 21(ID:disease_node_18952) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 55(ID:disease_node_16240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 102(ID:disease_node_16250) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 83(ID:disease_node_16171) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy Syndrome(ID:disease_node_18088) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 10B(ID:disease_node_18092) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Dermatosparaxis Type(ID:disease_node_18764) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 81(ID:disease_node_16172) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 6(ID:disease_node_15259) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1X(ID:disease_node_16898) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 23(ID:disease_node_16190) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 20(ID:disease_node_14296) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 9(ID:disease_node_18085) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 68(ID:disease_node_16184) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2C(ID:disease_node_16923) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dimethylglycine Dehydrogenase Deficiency(ID:disease_node_20523) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 2E(ID:disease_node_16921) (Disease)
Incoming r'ship SUBCLASS_OF to/from Endocrine-Cerebro-Osteodysplasia Syndrome(ID:disease_node_20325) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Spondylodysplastic Type 2(ID:disease_node_18774) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1F(ID:disease_node_20050) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 34(ID:disease_node_16204) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cystinosis(ID:disease_node_2358) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 20(ID:disease_node_18953) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 3(ID:disease_node_16223) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 40(ID:disease_node_16236) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 76(ID:disease_node_16176) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 37, Early-Onset With Striatal Lesions(ID:disease_node_17267) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 63(ID:disease_node_16264) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 16(ID:disease_node_14275) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniofacial Dysmorphism, Skeletal Anomalies, And Impaired Intellectual Development Syndrome 1(ID:disease_node_20274) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 35, Childhood-Onset(ID:disease_node_17268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Classic-Like 1(ID:disease_node_18766) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dyggve-Melchior-Clausen Disease(ID:disease_node_15667) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2K(ID:disease_node_18853) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cockayne Syndrome(ID:disease_node_2144) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 45(ID:disease_node_13671) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Iaa(ID:disease_node_20420) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ib(ID:disease_node_20419) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 49(ID:disease_node_16724) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 13 With Adult I Phenotype(ID:disease_node_13691) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Muscular Dystrophy 1B(ID:disease_node_17430) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Or Isolated Pituitary Hormone Deficiency 1(ID:disease_node_19692) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 33(ID:disease_node_13669) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 11(ID:disease_node_16744) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 47(ID:disease_node_16720) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation It(ID:disease_node_20403) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 14(ID:disease_node_16748) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 48(ID:disease_node_13697) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Deglycosylation 2(ID:disease_node_20472) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cleft Lip-Palate-Ectodermal Dysplasia Syndrome(ID:disease_node_20323) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Dyserythropoietic Anemia Type Ia(ID:disease_node_15274) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iin(ID:disease_node_20465) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ic(ID:disease_node_20418) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 35(ID:disease_node_13672) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 25(ID:disease_node_16755) (Disease)
Incoming r'ship SUBCLASS_OF to/from Compton-North Congenital Myopathy(ID:disease_node_18960) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Hereditary Endothelial Dystrophy Of Cornea(ID:disease_node_17120) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Hypotrichosis With Juvenile Macular Dystrophy(ID:disease_node_14196) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 26(ID:disease_node_16737) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 23(ID:disease_node_16728) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ik(ID:disease_node_20410) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2S(ID:disease_node_18849) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 52(ID:disease_node_16764) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4G(ID:disease_node_18828) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iik(ID:disease_node_20467) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iio(ID:disease_node_20464) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 3(ID:disease_node_18838) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 22(ID:disease_node_16730) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cone-Rod Dystrophy 22(ID:disease_node_16595) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Id(ID:disease_node_20417) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Muscular Dystrophy-Dystroglycanopathy Type A(ID:disease_node_17406) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 10(ID:disease_node_16745) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4K(ID:disease_node_18833) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Recessive Intermediate B(ID:disease_node_18818) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ih(ID:disease_node_20413) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 45(ID:disease_node_16721) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 1F(ID:disease_node_18871) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 13(ID:disease_node_16756) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 37(ID:disease_node_16729) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 46 Juvenile-Onset(ID:disease_node_13690) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 20(ID:disease_node_16747) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chondrodysplasia Punctata, Rhizomelic(ID:disease_node_9832) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 54(ID:disease_node_16762) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Fibrosis Of The Extraocular Muscles 5(ID:disease_node_20098) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 30(ID:disease_node_16752) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Muscular Dystrophy With Cataracts And Intellectual Disability(ID:disease_node_17422) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cone-Rod Dystrophy 21(ID:disease_node_16596) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 34(ID:disease_node_16731) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 38(ID:disease_node_16757) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4D(ID:disease_node_18834) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 39(ID:disease_node_16750) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 22 Multiple Types(ID:disease_node_13665) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 36(ID:disease_node_16743) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iil(ID:disease_node_20466) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ie(ID:disease_node_20416) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 27(ID:disease_node_16738) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation If(ID:disease_node_20415) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Im(ID:disease_node_20408) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Pituitary Hormone Deficiency 3(ID:disease_node_19690) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Iq(ID:disease_node_20405) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 36(ID:disease_node_13686) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2H(ID:disease_node_18854) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 12(ID:disease_node_16734) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 44(ID:disease_node_16765) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Glutamine Deficiency(ID:disease_node_20535) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Muscular Dystrophy Due To Integrin Alpha-7 Deficiency(ID:disease_node_17429) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cerebral Folate Receptor Alpha Deficiency(ID:disease_node_17079) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cd3Epsilon Deficiency(ID:disease_node_13324) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 29(ID:disease_node_16727) (Disease)
Incoming r'ship SUBCLASS_OF to/from Childhood-Onset Dystonia With Optic Atrophy And Basal Ganglia Abnormalities(ID:disease_node_14355) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ix(ID:disease_node_20400) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Malabsorptive Diarrhea 4(ID:disease_node_19333) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Diarrhea 7 With Exudative Enteropathy(ID:disease_node_19334) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 9 Multiple Types(ID:disease_node_13667) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 18(ID:disease_node_13695) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Il(ID:disease_node_20409) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 7(ID:disease_node_16740) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iii(ID:disease_node_20469) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ia(ID:disease_node_20421) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2X(ID:disease_node_18845) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 16(ID:disease_node_16754) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 56(ID:disease_node_16761) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iip(ID:disease_node_20463) (Disease)
Incoming r'ship SUBCLASS_OF to/from Common Variable Immunodeficiency(ID:disease_node_9017) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2P(ID:disease_node_18851) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ii(ID:disease_node_20412) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 57(ID:disease_node_16760) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chondrodysplasia With Joint Dislocations Gpapp Type(ID:disease_node_15641) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2T(ID:disease_node_18860) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4H(ID:disease_node_18832) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Pituitary Hormone Deficiency 2(ID:disease_node_19691) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 50(ID:disease_node_16723) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4E(ID:disease_node_18829) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ij(ID:disease_node_20411) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 8(ID:disease_node_16746) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ig(ID:disease_node_20414) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined D-2- And L-2-Hydroxyglutaric Aciduria(ID:disease_node_16044) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 40(ID:disease_node_16717) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4F(ID:disease_node_18831) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 15(ID:disease_node_16736) (Disease)
Incoming r'ship SUBCLASS_OF to/from Caroli Syndrome(ID:disease_node_15475) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Dyserythropoietic Anemia Type Iiib(ID:disease_node_15276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chediak-Higashi Syndrome(ID:disease_node_2023) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ip(ID:disease_node_20406) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cd3Gamma Deficiency(ID:disease_node_13323) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Diarrhea 5 With Tufting Enteropathy(ID:disease_node_19335) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iiq(ID:disease_node_20462) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2R(ID:disease_node_18859) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 33(ID:disease_node_16733) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 31(ID:disease_node_16739) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 11 Multiple Types(ID:disease_node_13684) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Leptin Deficiency(ID:disease_node_20248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Or Isolated Pituitary Growth Hormone Deficiency 7(ID:disease_node_19695) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4J(ID:disease_node_18835) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 51(ID:disease_node_16725) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 16 Multiple Types(ID:disease_node_13683) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cerebellar Atrophy, Visual Impairment, And Psychomotor Retardation(ID:disease_node_20268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 53(ID:disease_node_16763) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Iu(ID:disease_node_20402) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 43(ID:disease_node_16718) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Fibrosis Of The Extraocular Muscles 2(ID:disease_node_20100) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 19(ID:disease_node_16749) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 32(ID:disease_node_16735) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 17 Multiple Types(ID:disease_node_13663) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Recessive Intermediate D(ID:disease_node_18819) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 46(ID:disease_node_16719) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4C(ID:disease_node_18836) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Generalized Lipodystrophy(ID:disease_node_20148) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Recessive Intermediate C(ID:disease_node_18820) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Adrenal Insufficiency(ID:disease_node_17794) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 4B3(ID:disease_node_18830) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Iw(ID:disease_node_20401) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 42(ID:disease_node_16716) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 41(ID:disease_node_16715) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 35(ID:disease_node_16759) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 38(ID:disease_node_13688) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 19 Multiple Types(ID:disease_node_13670) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2Ee(ID:disease_node_18864) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iij(ID:disease_node_20468) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 24(ID:disease_node_16741) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 9(ID:disease_node_16751) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Ir(ID:disease_node_20404) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 48(ID:disease_node_16722) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cerebellofaciodental Syndrome(ID:disease_node_20271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 28(ID:disease_node_16753) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2A2B(ID:disease_node_18866) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 21(ID:disease_node_16758) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 44(ID:disease_node_13666) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 18(ID:disease_node_16742) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 17(ID:disease_node_16732) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation In(ID:disease_node_20407) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 5(ID:disease_node_17391) (Disease)
Incoming r'ship SUBCLASS_OF to/from Carbamoyl-Phosphate Synthase I Deficiency Disease(ID:disease_node_10151) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 2(ID:disease_node_17387) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 8(ID:disease_node_17390) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Recurrent Intrahepatic Cholestasis 1(ID:disease_node_17763) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 3(ID:disease_node_17389) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Hyaline Body Myopathy(ID:disease_node_18942) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Robinow Syndrome(ID:disease_node_17030) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 3(ID:disease_node_18044) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Pericentral Pigmentary Retinopathy(ID:disease_node_15825) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Craniometaphyseal Dysplasia(ID:disease_node_19043) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bh4-Deficient Hyperphenylalaninemia C(ID:disease_node_20528) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Type Iv Ehlers-Danlos Syndrome(ID:disease_node_18756) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brain Small Vessel Disease 3(ID:disease_node_20013) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Vocal Cord Paresis(ID:disease_node_18837) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Chronic Granulomatous Disease 5(ID:disease_node_20423) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Isolated Ectopia Lentis 2(ID:disease_node_13712) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Limb-Girdle Muscular Dystrophy(ID:disease_node_18885) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Chronic Granulomatous Disease 1(ID:disease_node_20427) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Chronic Granulomatous Disease 3(ID:disease_node_20425) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Thrombophilia Due To Protein S Deficiency(ID:disease_node_15583) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Centronuclear Myopathy(ID:disease_node_18929) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Whistling Face Syndrome(ID:disease_node_15784) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Progressive External Ophthalmoplegia 1(ID:disease_node_18045) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Dyskeratosis Congenita 6(ID:disease_node_13631) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Congenital Nystagmus(ID:disease_node_20555) (Disease)
Incoming r'ship SUBCLASS_OF to/from Canavan Disease(ID:disease_node_9337) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bent Bone Dysplasia Syndrome 2(ID:disease_node_19036) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Cutis Laxa Type Iib(ID:disease_node_17139) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 4(ID:disease_node_18051) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Cerebellar Ataxia(ID:disease_node_16008) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Congenital Bilateral Absence Of Vas Deferens(ID:disease_node_17152) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Spondyloepiphyseal Dysplasia Tarda(ID:disease_node_15689) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brown-Vialetto-Van Laere Syndrome 1(ID:disease_node_20388) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 3(ID:disease_node_15248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Alport Syndrome(ID:disease_node_19099) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 5(ID:disease_node_18043) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Dyskeratosis Congenita 3(ID:disease_node_13636) (Disease)
Incoming r'ship SUBCLASS_OF to/from Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency(ID:disease_node_20522) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Intellectual Developmental Disorder(ID:disease_node_16368) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 7(ID:disease_node_17384) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bilateral Frontoparietal Polymicrogyria(ID:disease_node_16161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Dyskeratosis Congenita 1(ID:disease_node_13640) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 6(ID:disease_node_17385) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brachyolmia-Amelogenesis Imperfecta Syndrome(ID:disease_node_20255) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 1(ID:disease_node_17388) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Emery-Dreifuss Muscular Dystrophy 3(ID:disease_node_18882) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bh4-Deficient Hyperphenylalaninemia B(ID:disease_node_20526) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Dyskeratosis Congenita 5(ID:disease_node_13633) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Distal Hereditary Motor Neuronopathy(ID:disease_node_18014) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Chronic Granulomatous Disease 2(ID:disease_node_20428) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Robinow Syndrome 2(ID:disease_node_17026) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Spondyloepiphyseal Dysplasia Tarda Leroy-Spranger Type(ID:disease_node_15690) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Osteopetrosis 4(ID:disease_node_17386) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bloom Syndrome(ID:disease_node_1624) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bardet-Biedl Syndrome(ID:disease_node_10716) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Woolly Hair 3(ID:disease_node_17465) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bernard-Soulier Syndrome(ID:disease_node_1515) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bh4-Deficient Hyperphenylalaninemia D(ID:disease_node_20527) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brittle Cornea Syndrome 2(ID:disease_node_18768) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Dyskeratosis Congenita 2(ID:disease_node_13638) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Cutis Laxa Type Ii Classic Type(ID:disease_node_17135) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brown-Vialetto-Van Laere Syndrome 2(ID:disease_node_20387) (Disease)
Incoming r'ship SUBCLASS_OF to/from Biotinidase Deficiency(ID:disease_node_10986) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Chronic Granulomatous Disease 4(ID:disease_node_20426) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2(ID:disease_node_15252) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bilateral Parasagittal Parieto-Occipital Polymicrogyria(ID:disease_node_16160) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 2(ID:disease_node_18036) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Hypophosphatemic Rickets(ID:disease_node_19039) (Disease)
Incoming r'ship SUBCLASS_OF to/from Becker Disease(ID:disease_node_15792) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Dyskeratosis Congenita 4(ID:disease_node_13634) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1H(ID:disease_node_18111) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria Type 9(ID:disease_node_19200) (Disease)
Incoming r'ship SUBCLASS_OF to/from 17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency(ID:disease_node_17168) (Disease)
Incoming r'ship SUBCLASS_OF to/from Antithrombin Iii Deficiency(ID:disease_node_10120) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis 8(ID:disease_node_19121) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 8B(ID:disease_node_17351) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 1(ID:disease_node_17358) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Hypomaturation Type 2A4(ID:disease_node_18113) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 7(ID:disease_node_17355) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 3C(ID:disease_node_18098) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amyotrophic Lateral Sclerosis Type 1(ID:disease_node_14063) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 6(ID:disease_node_17356) (Disease)
Incoming r'ship SUBCLASS_OF to/from Achondrogenesis Type Ib(ID:disease_node_15660) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arthrogryposis Multiplex Congenita(ID:disease_node_20565) (Disease)
Incoming r'ship SUBCLASS_OF to/from Afibrinogenemia(ID:disease_node_1054) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 2A6(ID:disease_node_18115) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alstrom Syndrome(ID:disease_node_12291) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aceruloplasminemia(ID:disease_node_17441) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anauxetic Dysplasia 2(ID:disease_node_15671) (Disease)
Incoming r'ship SUBCLASS_OF to/from Asphyxiating Thoracic Dystrophy 5(ID:disease_node_15731) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acromesomelic Dysplasia-4(ID:disease_node_15656) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria Type 3(ID:disease_node_19194) (Disease)
Incoming r'ship SUBCLASS_OF to/from Asphyxiating Thoracic Dystrophy 1(ID:disease_node_15734) (Disease)
Incoming r'ship SUBCLASS_OF to/from Albinism, Oculocutaneous(ID:disease_node_8609) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acheiropody(ID:disease_node_15682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atransferrinemia(ID:disease_node_17556) (Disease)
Incoming r'ship SUBCLASS_OF to/from Abetalipoproteinemia(ID:disease_node_5) (Disease)
Incoming r'ship SUBCLASS_OF to/from Asphyxiating Thoracic Dystrophy 3(ID:disease_node_15733) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acromesomelic Dysplasia, Hunter-Thompson Type(ID:disease_node_15658) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Hypomaturation Type 2A5(ID:disease_node_18112) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anemia, Dyserythropoietic, Congenital(ID:disease_node_1182) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria Type 5(ID:disease_node_19199) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1G(ID:disease_node_18109) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anauxetic Dysplasia 1(ID:disease_node_15672) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis 2(ID:disease_node_19127) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria Type 8(ID:disease_node_19201) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autoimmune Lymphoproliferative Syndrome Type 2B(ID:disease_node_13532) (Disease)
Incoming r'ship SUBCLASS_OF to/from Achromatopsia 7(ID:disease_node_19991) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1C(ID:disease_node_18105) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agenesis Of The Corpus Callosum With Peripheral Neuropathy(ID:disease_node_16096) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Hypomaturation Type 2A2(ID:disease_node_18101) (Disease)
Incoming r'ship SUBCLASS_OF to/from Asphyxiating Thoracic Dystrophy 4(ID:disease_node_15732) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 3(ID:disease_node_17357) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alopecia-Mental Retardation Syndrome 3(ID:disease_node_20303) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 4(ID:disease_node_17350) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acromesomelic Dysplasia, Grebe Type(ID:disease_node_15659) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agat Deficiency(ID:disease_node_20543) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1J(ID:disease_node_18116) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arc Syndrome(ID:disease_node_20360) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Hypomaturation Type 2A3(ID:disease_node_18114) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Standstill 2(ID:disease_node_20571) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1F(ID:disease_node_18110) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alkuraya-Kucinskas Syndrome(ID:disease_node_20384) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria With Cataracts, Neurologic Involvement And Neutropenia(ID:disease_node_19195) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria With Deafness, Encephalopathy, And Leigh-Like Syndrome(ID:disease_node_19198) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis 7(ID:disease_node_19122) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 7(ID:disease_node_17155) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 2A1(ID:disease_node_18104) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 9(ID:disease_node_17353) (Disease)
Incoming r'ship SUBCLASS_OF to/from Athabaskan Brainstem Dysgenesis Syndrome(ID:disease_node_20575) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 8(ID:disease_node_17156) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3Mc Syndrome(ID:disease_node_20340) (Disease)
Incoming r'ship SUBCLASS_OF to/from Achondrogenesis Type Ia(ID:disease_node_15661) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alopecia-Mental Retardation Syndrome 4(ID:disease_node_20304) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Hydroxyisobutryl-Coa Hydrolase Deficiency(ID:disease_node_20537) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alopecia-Mental Retardation Syndrome 1(ID:disease_node_20305) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylcrotonyl-Coa Carboxylase Deficiency(ID:disease_node_18811) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amed Syndrome(ID:disease_node_19185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alacrima, Achalasia, And Impaired Intellectual Development Syndrome(ID:disease_node_13251) (Disease)
Incoming r'ship SUBCLASS_OF to/from Antley-Bixler Syndrome With Disordered Steroidogenesis(ID:disease_node_13625) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alpha-2-Plasmin Inhibitor Deficiency(ID:disease_node_19431) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 2(ID:disease_node_17359) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anemia, Sickle Cell(ID:disease_node_1204) (Disease)
Incoming r'ship SUBCLASS_OF to/from 2-Aminoadipic 2-Oxoadipic Aciduria(ID:disease_node_20521) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autoimmune Lymphoproliferative Syndrome Type 3(ID:disease_node_13530) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease)

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Grayu

Autosomal Recessive Disease

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Disease Properties

Associated Connections 1307

Disease Connections 1307