Autosomal Domit Disease

Disease ID: disease_node_13255

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Subclassof	DOID_0050739
Data Source	DOID
Doid Label	autosomal domit disease
Doid Description	An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.
Disease Node Id	disease_node_13255
Doid Id	DOID_0050736
Label	Autosomal Domit Disease

Incoming r'ship SUBCLASS_OF to/from Atypical Autosomal Domit Adult-Onset Demyelinating Leukodystrophy(ID:disease_node_19957) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zttk Syndrome(ID:disease_node_20153) (Disease)
Incoming r'ship SUBCLASS_OF to/from Teebi Hypertelorism Syndrome 1(ID:disease_node_20103) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tubular Aggregate Myopathy 1(ID:disease_node_18986) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tubular Aggregate Myopathy 2(ID:disease_node_18973) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sting-Associated Vasculopathy With Onset In Infancy(ID:disease_node_20039) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vissers-Bodmer Syndrome(ID:disease_node_20085) (Disease)
Incoming r'ship SUBCLASS_OF to/from Williams Syndrome(ID:disease_node_9850) (Disease)
Incoming r'ship SUBCLASS_OF to/from Trichorhinophalangeal Syndrome Type Iii(ID:disease_node_20114) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tuberous Sclerosis(ID:disease_node_7665) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 1(ID:disease_node_17281) (Disease)
Incoming r'ship SUBCLASS_OF to/from Striatal Degeneration 2(ID:disease_node_16123) (Disease)
Incoming r'ship SUBCLASS_OF to/from Thomsen Disease(ID:disease_node_15791) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndactyly Type 1(ID:disease_node_13622) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 6(ID:disease_node_17280) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vertebral Hypersegmentation And Orofacial Anomalies(ID:disease_node_20133) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tatton-Brown-Rahman Syndrome(ID:disease_node_16361) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vascular Type Ehlers-Danlos Syndrome(ID:disease_node_18757) (Disease)
Incoming r'ship SUBCLASS_OF to/from Watson Syndrome(ID:disease_node_19062) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tarsal-Carpal Coalition Syndrome(ID:disease_node_15746) (Disease)
Incoming r'ship SUBCLASS_OF to/from Thrombophilia Due To Thrombin Defect(ID:disease_node_17041) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tnf Receptor–Associated Periodic Syndrome(ID:disease_node_15588) (Disease)
Incoming r'ship SUBCLASS_OF to/from Typical Adult-Onset Autosomal Domit Demyelinating Leukodystrophy(ID:disease_node_19956) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 2(ID:disease_node_19908) (Disease)
Incoming r'ship SUBCLASS_OF to/from White Sponge Nevus 1(ID:disease_node_20088) (Disease)
Incoming r'ship SUBCLASS_OF to/from Stickler Syndrome 2(ID:disease_node_20112) (Disease)
Incoming r'ship SUBCLASS_OF to/from Telangiectasia, Hereditary Hemorrhagic(ID:disease_node_7298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Type 1 Diabetes Mellitus 2(ID:disease_node_14379) (Disease)
Incoming r'ship SUBCLASS_OF to/from Thrombophilia Due To Hrg Deficiency(ID:disease_node_17042) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 4(ID:disease_node_14349) (Disease)
Incoming r'ship SUBCLASS_OF to/from Variant Abeta2M Amyloidosis(ID:disease_node_17484) (Disease)
Incoming r'ship SUBCLASS_OF to/from Stickler Syndrome 1(ID:disease_node_20110) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vertebral Anomalies And Variable Endocrine And T-Cell Dysfunction(ID:disease_node_20141) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ullrich Congenital Muscular Dystrophy(ID:disease_node_17423) (Disease)
Incoming r'ship SUBCLASS_OF to/from White Sponge Nevus 2(ID:disease_node_20087) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 13(ID:disease_node_14351) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sweeney-Cox Syndrome(ID:disease_node_20115) (Disease)
Incoming r'ship SUBCLASS_OF to/from Steatocystoma Multiplex(ID:disease_node_12898) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torsion Dystonia 7(ID:disease_node_14336) (Disease)
Incoming r'ship SUBCLASS_OF to/from Transthyretin Amyloidosis(ID:disease_node_17489) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinal Macular Dystrophy(ID:disease_node_16564) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 7(ID:disease_node_15936) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rhabdoid Tumor Predisposition Syndrome(ID:disease_node_20129) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 3(ID:disease_node_15215) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sorsby'S Fundus Dystrophy(ID:disease_node_20035) (Disease)
Incoming r'ship SUBCLASS_OF to/from Solitary Median Maxillary Central Incisor(ID:disease_node_18126) (Disease)
Incoming r'ship SUBCLASS_OF to/from Renal Hypomagnesemia 7, With Or Without Dilated Cardiomyopathy(ID:disease_node_17550) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 8(ID:disease_node_15935) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 83(ID:disease_node_15801) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 36(ID:disease_node_15172) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 15(ID:disease_node_15928) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 12(ID:disease_node_15931) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sclerosteosis 2(ID:disease_node_13721) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 3(ID:disease_node_15940) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia Nishimura Type(ID:disease_node_15685) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 2(ID:disease_node_15218) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 5(ID:disease_node_15938) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 7(ID:disease_node_16065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 60(ID:disease_node_15832) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepimetaphyseal Dysplasia With Joint Laxity Type 2(ID:disease_node_15665) (Disease)
Incoming r'ship SUBCLASS_OF to/from Speech-Language Disorder-1(ID:disease_node_15862) (Disease)
Incoming r'ship SUBCLASS_OF to/from Saul-Wilson Syndrome(ID:disease_node_15700) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spastic Ataxia 1(ID:disease_node_16064) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinal Arterial Tortuosity(ID:disease_node_20184) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 6(ID:disease_node_15937) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 8(ID:disease_node_15234) (Disease)
Incoming r'ship SUBCLASS_OF to/from Situs Inversus(ID:disease_node_6959) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia 1(ID:disease_node_18057) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 2(ID:disease_node_15941) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rubinstein-Taybi Syndrome(ID:disease_node_6709) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 1(ID:disease_node_15942) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloperipheral Dysplasia(ID:disease_node_15646) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sotos Syndrome 2(ID:disease_node_15602) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 11(ID:disease_node_15932) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 87(ID:disease_node_15798) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 4(ID:disease_node_15939) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rippling Muscle Disease 2(ID:disease_node_15793) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spinal Muscular Atrophy With Lower Extremity Predomit(ID:disease_node_18024) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 89(ID:disease_node_15796) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short Stature, Facial Dysmorphism, And Skeletal Anomalies With Or Without Cardiac Anomalies 1(ID:disease_node_20135) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 63(ID:disease_node_15803) (Disease)
Incoming r'ship SUBCLASS_OF to/from Renal Coloboma Syndrome(ID:disease_node_20077) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 11(ID:disease_node_15223) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 10(ID:disease_node_15933) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 10(ID:disease_node_15227) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia Stanescu Type(ID:disease_node_15694) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepimetaphyseal Dysplasia, Strudwick Type(ID:disease_node_15673) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 32(ID:disease_node_15170) (Disease)
Incoming r'ship SUBCLASS_OF to/from Split Hand-Foot Malformation 1(ID:disease_node_15709) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia Maroteaux Type(ID:disease_node_15687) (Disease)
Incoming r'ship SUBCLASS_OF to/from Revesz Syndrome(ID:disease_node_13629) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 12(ID:disease_node_15232) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 70(ID:disease_node_15843) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spermatogenic Failure 4(ID:disease_node_15229) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spinal Muscular Atrophy, Jokela Type(ID:disease_node_18023) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sotos Syndrome 1(ID:disease_node_15601) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 8(ID:disease_node_16139) (Disease)
Incoming r'ship SUBCLASS_OF to/from Posterior Polymorphous Corneal Dystrophy 2(ID:disease_node_17145) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 17(ID:disease_node_16137) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paroxysmal Nonkinesigenic Dyskinesia 3(ID:disease_node_17263) (Disease)
Incoming r'ship SUBCLASS_OF to/from Poor Metabolism Of Thiopurines 2(ID:disease_node_17535) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paraganglioma(ID:disease_node_5870) (Disease)
Incoming r'ship SUBCLASS_OF to/from Papa Syndrome(ID:disease_node_20116) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 3(ID:disease_node_17056) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progeria(ID:disease_node_6328) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 15(ID:disease_node_17058) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proximal Symphalangism(ID:disease_node_19033) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Familial Heart Block Type Ia(ID:disease_node_20041) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pancreatic Hypoplasia-Diabetes-Congenital Heart Disease Syndrome(ID:disease_node_20025) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pallister-Hall Syndrome(ID:disease_node_12001) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pcwh Syndrome(ID:disease_node_20080) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 1(ID:disease_node_16140) (Disease)
Incoming r'ship SUBCLASS_OF to/from Permanent Neonatal Diabetes Mellitus(ID:disease_node_17245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Protein C Deficiency(ID:disease_node_10116) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paget'S Disease Of Bone 3(ID:disease_node_13718) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 5(ID:disease_node_17216) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 16(ID:disease_node_17065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Autosomal Domit Microcephaly 18(ID:disease_node_19305) (Disease)
Incoming r'ship SUBCLASS_OF to/from Piebaldism(ID:disease_node_8616) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteosome-Associated Autoinflammatory Syndrome 2(ID:disease_node_15598) (Disease)
Incoming r'ship SUBCLASS_OF to/from Preaxial Polydactyly Type Iv(ID:disease_node_20138) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 7(ID:disease_node_17214) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paget'S Disease Of Bone 4(ID:disease_node_13717) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pemphigus, Benign Familial(ID:disease_node_8738) (Disease)
Incoming r'ship SUBCLASS_OF to/from Prothrombin Thrombophilia(ID:disease_node_17043) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 9(ID:disease_node_17053) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 6(ID:disease_node_17215) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ciliary Dyskinesia 43(ID:disease_node_14675) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 3(ID:disease_node_16141) (Disease)
Incoming r'ship SUBCLASS_OF to/from Posterior Polymorphous Corneal Dystrophy 4(ID:disease_node_17147) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 16(ID:disease_node_17205) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pulmonary Venoocclusive Disease 1(ID:disease_node_20089) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pachyonychia Congenita(ID:disease_node_11715) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 21(ID:disease_node_16135) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 12(ID:disease_node_17054) (Disease)
Incoming r'ship SUBCLASS_OF to/from Punctate Palmoplantar Keratoderma Type Ii(ID:disease_node_19359) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 22(ID:disease_node_16136) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 14(ID:disease_node_17063) (Disease)
Incoming r'ship SUBCLASS_OF to/from Posterior Polymorphous Corneal Dystrophy 1(ID:disease_node_17146) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 11(ID:disease_node_17210) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 4(ID:disease_node_16138) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Pigmented Nodular Adrenocortical Disease 4(ID:disease_node_14165) (Disease)
Incoming r'ship SUBCLASS_OF to/from Platelet-Type Bleeding Disorder 20(ID:disease_node_17057) (Disease)
Incoming r'ship SUBCLASS_OF to/from Puberty, Precocious(ID:disease_node_6420) (Disease)
Incoming r'ship SUBCLASS_OF to/from Polycystic Kidney Diseases(ID:disease_node_4502) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progressive Myoclonus Epilepsy 7(ID:disease_node_16298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paget'S Disease Of Bone 6(ID:disease_node_13715) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pelger-Huet Anomaly(ID:disease_node_5946) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 3(ID:disease_node_17218) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paroxysmal Nonkinesigenic Dyskinesia 1(ID:disease_node_14357) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paget'S Disease Of Bone 2(ID:disease_node_13719) (Disease)
Incoming r'ship SUBCLASS_OF to/from Preaxial Polydactyly Ii(ID:disease_node_20136) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisome Biogenesis Disorder 4B(ID:disease_node_17524) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myopathy, Central Core(ID:disease_node_10605) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 3(ID:disease_node_15629) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 2(ID:disease_node_15627) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 8(ID:disease_node_19052) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofacial Cleft 13(ID:disease_node_14028) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oculopharyngodistal Myopathy 4(ID:disease_node_18967) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 5(ID:disease_node_18451) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Epiphyseal Dysplasia 3(ID:disease_node_15637) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mobius Syndrome(ID:disease_node_10509) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Ceroid Lipofuscinosis 4(ID:disease_node_15951) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myoclonic Dystonia 34(ID:disease_node_17266) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 10(ID:disease_node_19050) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Atrophy 8(ID:disease_node_17291) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Atrophy 1(ID:disease_node_17290) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ocular Albinism With Sensorineural Deafness(ID:disease_node_19184) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 7(ID:disease_node_18449) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myoclonic-Atonic Epilepsy(ID:disease_node_13395) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nevoid Basal Cell Carcinoma Syndrome 1(ID:disease_node_20139) (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 Oculopharyngodistal Myopathy 2(ID:disease_node_18969) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nemaline Myopathy 5C(ID:disease_node_18934) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 5(ID:disease_node_18981) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 12(ID:disease_node_19047) (Disease)
Incoming r'ship SUBCLASS_OF to/from Otosclerosis(ID:disease_node_5801;disease_node_17729) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 1(ID:disease_node_18454) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oculopharyngodistal Myopathy 3(ID:disease_node_18968) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ovarian Dysgenesis 8(ID:disease_node_14938) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myositis Ossificans(ID:disease_node_5377) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Epiphyseal Dysplasia 6(ID:disease_node_15638) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Atrophy 10(ID:disease_node_17293) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephrotic Syndrome Type 4(ID:disease_node_19083) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurooculocardiogenitourinary Syndrome(ID:disease_node_20019) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myoclonic Dystonia 26(ID:disease_node_14352) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurofibromatoses(ID:disease_node_9133) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 13(ID:disease_node_19049) (Disease)
Incoming r'ship SUBCLASS_OF to/from Overhydrated Hereditary Stomatocytosis(ID:disease_node_15317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 8(ID:disease_node_18448) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder 6(ID:disease_node_18450) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nail-Patella Syndrome(ID:disease_node_5399) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 6(ID:disease_node_18980) (Disease)
Incoming r'ship SUBCLASS_OF to/from Otospondylomegaepiphyseal Dysplasia, Autosomal Domit(ID:disease_node_15655) (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 2(ID:disease_node_18983) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 9(ID:disease_node_19051) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta(ID:disease_node_5768) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonautoimmune Hyperthyroidism(ID:disease_node_14387) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myopathies, Structural, Congenital(ID:disease_node_10806) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Types Of Congenital Heart Defects 6(ID:disease_node_20067) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodevelopmental Disorder With Involuntary Movements(ID:disease_node_16712) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myoclonic Dystonia 11(ID:disease_node_14354) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oblique Facial Clefting 1(ID:disease_node_14031) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Synostoses Syndrome(ID:disease_node_15741) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neuronal Intranuclear Inclusion Disease(ID:disease_node_16099) (Disease)
Incoming r'ship SUBCLASS_OF to/from Monilethrix(ID:disease_node_12277) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Nerve Hypoplasia(ID:disease_node_433) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Endocrine Neoplasia Type 2A(ID:disease_node_9794) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofacial Cleft 6(ID:disease_node_14030) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Endocrine Neoplasia Type 2B(ID:disease_node_9799) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 5(ID:disease_node_15624) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nicolaides-Baraitser Syndrome(ID:disease_node_20079) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 7(ID:disease_node_19053) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Endocrine Neoplasia Type 1(ID:disease_node_9762) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 4(ID:disease_node_15628) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 1(ID:disease_node_19054) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noo Syndrome 11(ID:disease_node_19048) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myofibrillar Myopathy 4(ID:disease_node_18982) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Atrophy, Spinal(ID:disease_node_5313) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oculopharyngodistal Myopathy 1(ID:disease_node_18970) (Disease)
Incoming r'ship SUBCLASS_OF to/from Optic Atrophy 12(ID:disease_node_17294) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Epiphyseal Dysplasia 2(ID:disease_node_15639) (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 Nonsyndromic Congenital Nail Disorder 2(ID:disease_node_18453) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myoclonic Dystonia 15(ID:disease_node_14353) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 16(ID:disease_node_16875) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lacrimoauriculodentodigital Syndrome 2(ID:disease_node_20094) (Disease)
Incoming r'ship SUBCLASS_OF to/from Langer-Giedion Syndrome(ID:disease_node_8482) (Disease)
Incoming r'ship SUBCLASS_OF to/from Megalencephalic Leukoencephalopathy With Subcortical Cysts 2B(ID:disease_node_19921) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mandibulofacial Dysostosis(ID:disease_node_4988) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kleefstra Syndrome 2(ID:disease_node_17117) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 14(ID:disease_node_16877) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leucine-Sensitive Hypoglycemia Of Infancy(ID:disease_node_16860) (Disease)
Incoming r'ship SUBCLASS_OF to/from Malignant Hyperthermia(ID:disease_node_4965) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meier-Gorlin Syndrome 6(ID:disease_node_20117) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 15(ID:disease_node_16876) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitchell Syndrome(ID:disease_node_17531) (Disease)
Incoming r'ship SUBCLASS_OF to/from Maturity-Onset Diabetes Of The Young(ID:disease_node_17248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 1(ID:disease_node_19266) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 9 With Complex Brainstem Malformation(ID:disease_node_19274) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mandibulofacial Dysostosis, Guion-Almeida Type(ID:disease_node_20125) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lacrimoauriculodentodigital Syndrome 3(ID:disease_node_20092) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lissencephaly 10(ID:disease_node_19273) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Feil Syndrome 1(ID:disease_node_17383) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meesmann Corneal Dystrophy 1(ID:disease_node_17143) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Feil Syndrome 3(ID:disease_node_17381) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis With Early-Onset Deafness(ID:disease_node_17994) (Disease)
Incoming r'ship SUBCLASS_OF to/from Li-Fraumeni Syndrome(ID:disease_node_8936) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 4A(ID:disease_node_16798) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome 12A(ID:disease_node_16823) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations(ID:disease_node_16367) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lacrimoauriculodentodigital Syndrome 1(ID:disease_node_20095) (Disease)
Incoming r'ship SUBCLASS_OF to/from Koolen De Vries Syndrome(ID:disease_node_20165) (Disease)
Incoming r'ship SUBCLASS_OF to/from Metaphyseal Dysplasia-Maxillary Hypoplasia-Brachydactyly Syndrome(ID:disease_node_15647) (Disease)
Incoming r'ship SUBCLASS_OF to/from Marsili Syndrome(ID:disease_node_15874) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meesmann Corneal Dystrophy 2(ID:disease_node_17142) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lipodystrophy, Familial Partial(ID:disease_node_11541) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 8(ID:disease_node_16879) (Disease)
Incoming r'ship SUBCLASS_OF to/from Miura Type Epiphyseal Chondrodysplasia(ID:disease_node_15719) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 13(ID:disease_node_16878) (Disease)
Incoming r'ship SUBCLASS_OF to/from Macular Degeneration(ID:disease_node_4942) (Disease)
Incoming r'ship SUBCLASS_OF to/from Loeys-Dietz Syndrome(ID:disease_node_12127) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 1(ID:disease_node_16880) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leopard Syndrome(ID:disease_node_11206) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kinsship Syndrome(ID:disease_node_19994) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 27B(ID:disease_node_20016) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 10(ID:disease_node_16645) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inclusion Body Myopathy And Brain White Matter Abnormalities(ID:disease_node_20029) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 88(ID:disease_node_16676) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 3(ID:disease_node_20026) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 90B(ID:disease_node_16673) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 29(ID:disease_node_16628) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 9 With Or Without Anosmia(ID:disease_node_17185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 21 With Or Without Anosmia(ID:disease_node_17177) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 11(ID:disease_node_14199) (Disease)
Incoming r'ship SUBCLASS_OF to/from Juvenile Polyposis-Hereditary Hemorrhagic Telangiectasia Syndrome(ID:disease_node_20185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 1A(ID:disease_node_19416) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 3(ID:disease_node_14206) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intellectual Disability-Severe Speech Delay-Mild Dysmorphism Syndrome(ID:disease_node_16363) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 6(ID:disease_node_16660) (Disease)
Incoming r'ship SUBCLASS_OF to/from Idiopathic Pulmonary Fibrosis(ID:disease_node_12012) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 7(ID:disease_node_19425) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 6(ID:disease_node_19937) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 20 With Or Without Anosmia(ID:disease_node_17188) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 13(ID:disease_node_20008) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hot Water Epilepsy 1(ID:disease_node_16302) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Mixed Polyposis Syndrome 2(ID:disease_node_19228) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Breast And Ovarian Cancer Syndrome(ID:disease_node_12864) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 13(ID:disease_node_16642) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory And Autonomic Neuropathy Type 1C(ID:disease_node_19413) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Lymphedema Id(ID:disease_node_18238) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 12(ID:disease_node_14198) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inflammatory Bowel Disease 30(ID:disease_node_14187) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2(ID:disease_node_20028) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperekplexia(ID:disease_node_150) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ichthyosis Vulgaris(ID:disease_node_8589) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 17 With Or Without Anosmia(ID:disease_node_17191) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 72A(ID:disease_node_16654) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 15 With Or Without Anosmia(ID:disease_node_17195) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 19(ID:disease_node_16636) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 1(ID:disease_node_14208) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory Neuropathy Type 1E(ID:disease_node_19422) (Disease)
Incoming r'ship SUBCLASS_OF to/from Juvenile Amyotrophic Lateral Sclerosis Type 27(ID:disease_node_14038) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intrahepatic Cholestasis Of Pregcy 3(ID:disease_node_17764) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory Neuropathy Type 1F(ID:disease_node_19415) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 41(ID:disease_node_16686) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intracranial Berry Aneurysm 3(ID:disease_node_15449) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 37(ID:disease_node_16691) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 11B(ID:disease_node_20007) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory Neuropathy Type 1D(ID:disease_node_19414) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 16 With Or Without Anosmia(ID:disease_node_17190) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ichthyosis Bullosa Of Siemens(ID:disease_node_11724) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inflammatory Bowel Disease 29(ID:disease_node_14186) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Lymphedema Ib(ID:disease_node_18236) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyperekplexia 3(ID:disease_node_20161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 38(ID:disease_node_16690) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Lymphedema Ic(ID:disease_node_18239) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intrahepatic Cholestasis Of Pregcy 1(ID:disease_node_17765) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 14 With Or Without Anosmia(ID:disease_node_17183) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kenny-Caffey Syndrome Type 2(ID:disease_node_15652) (Disease)
Incoming r'ship SUBCLASS_OF to/from Iridogoniodysgenesis Syndrome(ID:disease_node_17298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 15A(ID:disease_node_13298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Mitochondrial Myopathy(ID:disease_node_18037) (Disease)
Incoming r'ship SUBCLASS_OF to/from Holoprosencephaly 12(ID:disease_node_13585) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 36(ID:disease_node_16692) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spherocytosis Type 4(ID:disease_node_15278) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 3 With Or Without Anosmia(ID:disease_node_17178) (Disease)
Incoming r'ship SUBCLASS_OF to/from Itm2B-Related Cerebral Amyloid Angiopathy 1(ID:disease_node_17492) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 2 With Or Without Anosmia(ID:disease_node_17187) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 70(ID:disease_node_13306) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 60(ID:disease_node_13299) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 49(ID:disease_node_20001) (Disease)
Incoming r'ship SUBCLASS_OF to/from Interstitial Lung Disease 1(ID:disease_node_14636) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 12(ID:disease_node_16643) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Elevated Serum Creatine Phosphokinase Levels(ID:disease_node_17532) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Diffuse Gastric Cancer(ID:disease_node_19583) (Disease)
Incoming r'ship SUBCLASS_OF to/from Jansen'S Metaphyseal Chondrodysplasia(ID:disease_node_15678) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile-Onset Distal Myopathy(ID:disease_node_18922) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spherocytosis Type 1(ID:disease_node_15281) (Disease)
Incoming r'ship SUBCLASS_OF to/from Interstitial Lung Disease 2(ID:disease_node_14635) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 32A(ID:disease_node_20187) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 4 With Or Without Anosmia(ID:disease_node_17193) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Lymphedema Ia(ID:disease_node_18237) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 8(ID:disease_node_16648) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 16(ID:disease_node_19928) (Disease)
Incoming r'ship SUBCLASS_OF to/from Job Syndrome(ID:disease_node_4401) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 39(ID:disease_node_20015) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 31C(ID:disease_node_20017) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 4(ID:disease_node_14205) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 19 With Or Without Anosmia(ID:disease_node_17180) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 9A(ID:disease_node_16647) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 1(ID:disease_node_20027) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 4(ID:disease_node_16687) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 31A(ID:disease_node_20018) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 80(ID:disease_node_16625) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypoinsulinemic Hypoglycemia With Hemihypertrophy(ID:disease_node_16852) (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 Hypogonadotropic Hypogonadism 5 With Or Without Anosmia(ID:disease_node_17186) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 13(ID:disease_node_14197) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotonia, Ataxia, And Delayed Development Syndrome(ID:disease_node_20164) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 17(ID:disease_node_16638) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intracranial Berry Aneurysm 1(ID:disease_node_15451) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis 2(ID:disease_node_14207) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 19(ID:disease_node_19933) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 25(ID:disease_node_19932) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 36(ID:disease_node_13302) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 31(ID:disease_node_16627) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 22(ID:disease_node_19931) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spherocytosis Type 2(ID:disease_node_15280) (Disease)
Incoming r'ship SUBCLASS_OF to/from Juvenile Glaucoma(ID:disease_node_14331) (Disease)
Incoming r'ship SUBCLASS_OF to/from Itm2B-Related Cerebral Amyloid Angiopathy 2(ID:disease_node_17491) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 3A(ID:disease_node_16688) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 73(ID:disease_node_16653) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome(ID:disease_node_20037) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 33(ID:disease_node_16695) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 42(ID:disease_node_16685) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 6 With Or Without Anosmia(ID:disease_node_17184) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 79A(ID:disease_node_16678) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 90A(ID:disease_node_16674) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 73B With Defective Neutrophil Chemotaxis And Lymphopenia(ID:disease_node_13334) (Disease)
Incoming r'ship SUBCLASS_OF to/from Holoprosencephaly 11(ID:disease_node_13584) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypomyelinating Leukodystrophy 24(ID:disease_node_19927) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 7(ID:disease_node_16609) (Disease)
Incoming r'ship SUBCLASS_OF to/from Holoprosencephaly 1(ID:disease_node_13583) (Disease)
Incoming r'ship SUBCLASS_OF to/from Episodic Kinesigenic Dyskinesia 3(ID:disease_node_17269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Erythrocytosis 3(ID:disease_node_15332) (Disease)
Incoming r'ship SUBCLASS_OF to/from Exudative Vitreoretinopathy 7(ID:disease_node_17037) (Disease)
Incoming r'ship SUBCLASS_OF to/from Essential Tremor 2(ID:disease_node_16701) (Disease)
Incoming r'ship SUBCLASS_OF to/from Finnish Type Amyloidosis(ID:disease_node_17122) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 7(ID:disease_node_13372) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Or Diffuse Nonepidermolytic Palmoplantar Keratoderma(ID:disease_node_19363) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hajdu-Cheney Syndrome(ID:disease_node_11081) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis Et Progressiva 6(ID:disease_node_19132) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group R(ID:disease_node_15294) (Disease)
Incoming r'ship SUBCLASS_OF to/from Geleophysic Dysplasia 3(ID:disease_node_15705) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fibrochondrogenesis 2(ID:disease_node_15679) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gata2 Deficiency(ID:disease_node_379) (Disease)
Incoming r'ship SUBCLASS_OF to/from Grn-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions(ID:disease_node_18035) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 3(ID:disease_node_16284) (Disease)
Incoming r'ship SUBCLASS_OF to/from Harel-Yoon Syndrome(ID:disease_node_20086) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Cold Autoinflammatory Syndrome 4(ID:disease_node_15590) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Focal Epilepsy With Variable Foci(ID:disease_node_13377) (Disease)
Incoming r'ship SUBCLASS_OF to/from Essential Tremor 6(ID:disease_node_16703) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 7(ID:disease_node_16285) (Disease)
Incoming r'ship SUBCLASS_OF to/from Giant Axonal Neuropathy 2(ID:disease_node_13536) (Disease)
Incoming r'ship SUBCLASS_OF to/from Exudative Vitreoretinopathy 6(ID:disease_node_17039) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 4(ID:disease_node_16286) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycosuria, Renal(ID:disease_node_3544) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Erythrocytosis 5(ID:disease_node_15333) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis Et Progressiva 2(ID:disease_node_19136) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Nonepidermolytic Palmoplantar Keratoderma 2(ID:disease_node_19364) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 3(ID:disease_node_16858) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gray Platelet Syndrome(ID:disease_node_12095) (Disease)
Incoming r'ship SUBCLASS_OF to/from Growth Hormone Insensitivity Syndrome With Immune Dysregulation 2(ID:disease_node_20106) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Renotubular Syndrome 4(ID:disease_node_19159) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Behcet-Like Autoinflammatory Syndrome(ID:disease_node_15593) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frasier Syndrome(ID:disease_node_11506) (Disease)
Incoming r'ship SUBCLASS_OF to/from Heinz Body Anemia(ID:disease_node_15261) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Visceral Amyloidosis(ID:disease_node_17490) (Disease)
Incoming r'ship SUBCLASS_OF to/from Foveal Hypoplasia 1(ID:disease_node_20194) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolytic Palmoplantar Keratoderma 2(ID:disease_node_19356) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 6(ID:disease_node_16857) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Cold Autoinflammatory Syndrome 3(ID:disease_node_15591) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Multiple Lipomatosis(ID:disease_node_161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Flatfoot(ID:disease_node_3269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Episodic Ataxia Type 9(ID:disease_node_16049) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 1(ID:disease_node_16289) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Partial Lipodystrophy Type 4(ID:disease_node_20142) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolytic Palmoplantar Keratoderma 1(ID:disease_node_19355) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolytic Hyperkeratosis 1(ID:disease_node_19968) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis Et Progressiva 3(ID:disease_node_19135) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 6(ID:disease_node_16283) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adenomatous Polyposis 1(ID:disease_node_17035) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Nonepidermolytic Palmoplantar Keratoderma 1(ID:disease_node_19365) (Disease)
Incoming r'ship SUBCLASS_OF to/from Essential Tremor 5(ID:disease_node_16698) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Erythrocytosis 1(ID:disease_node_15334) (Disease)
Incoming r'ship SUBCLASS_OF to/from Exostoses, Multiple Hereditary(ID:disease_node_3085) (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 3(ID:disease_node_19160) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 1(ID:disease_node_16855) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Gestational Hyperthyroidism(ID:disease_node_14386) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Segmental Glomerulosclerosis 8(ID:disease_node_15776) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Episodic Pain Syndrome 1(ID:disease_node_19411) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 1(ID:disease_node_13375) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 5(ID:disease_node_16854) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 2(ID:disease_node_13368) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gingival Fibromatosis 5(ID:disease_node_18077) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 8(ID:disease_node_13369) (Disease)
Incoming r'ship SUBCLASS_OF to/from Essential Tremor 1(ID:disease_node_16702) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Renotubular Syndrome 1(ID:disease_node_19162) (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 Temporal Lobe Epilepsy 6(ID:disease_node_13374) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Cold Autoinflammatory Syndrome 1(ID:disease_node_15592) (Disease)
Incoming r'ship SUBCLASS_OF to/from Geleophysic Dysplasia 2(ID:disease_node_15706) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Segmental Glomerulosclerosis 7(ID:disease_node_15777) (Disease)
Incoming r'ship SUBCLASS_OF to/from Essential Tremor 4(ID:disease_node_16699) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Progressive Hyperpigmentation With Or Without Hypopigmentation(ID:disease_node_20036) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Episodic Pain Syndrome 2(ID:disease_node_19410) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hand-Foot-Genital Syndrome(ID:disease_node_20158) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Apolipoprotein A5 Deficiency(ID:disease_node_16847) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Episodic Pain Syndrome 3(ID:disease_node_19409) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hypocalciuric Hypercalcemia(ID:disease_node_17444) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frontometaphyseal Dysplasia 2(ID:disease_node_15702) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 4(ID:disease_node_13370) (Disease)
Incoming r'ship SUBCLASS_OF to/from Episodic Kinesigenic Dyskinesia 1(ID:disease_node_14356) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Segmental Glomerulosclerosis 1(ID:disease_node_15779) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hyperinsulinemic Hypoglycemia 2(ID:disease_node_16856) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Temporal Lobe Epilepsy 3(ID:disease_node_13373) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Adult Myoclonic Epilepsy 2(ID:disease_node_16287) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental Dysplasia Of The Hip 1(ID:disease_node_15721) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 98(ID:disease_node_16254) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 74(ID:disease_node_16178) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 4A(ID:disease_node_18958) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Dd(ID:disease_node_16895) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 2C(ID:disease_node_18948) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 96(ID:disease_node_16261) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 11(ID:disease_node_15311) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 17(ID:disease_node_16213) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 87(ID:disease_node_16168) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 32(ID:disease_node_16189) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Ii(ID:disease_node_16892) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 19(ID:disease_node_15314) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 56(ID:disease_node_16241) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Myopathy 3(ID:disease_node_18917) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 45(ID:disease_node_16235) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 2B3(ID:disease_node_15786) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 43(ID:disease_node_16216) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Nn(ID:disease_node_16910) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Ll(ID:disease_node_16925) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 1B(ID:disease_node_14295) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dehydrated Hereditary Stomatocytosis 1(ID:disease_node_15284) (Disease)
Incoming r'ship SUBCLASS_OF to/from Crouzon Syndrome-Acanthosis Nigricans Syndrome(ID:disease_node_19032) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 65(ID:disease_node_16233) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolysis Bullosa Simplex Generalized Type(ID:disease_node_14233) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nystagmus 7(ID:disease_node_20024) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolysis Bullosa Simplex Localized Type(ID:disease_node_14234) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 72(ID:disease_node_16180) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 17(ID:disease_node_15316) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cornelia De Lange Syndrome 6(ID:disease_node_19097) (Disease)
Incoming r'ship SUBCLASS_OF to/from Domit Optic Atrophy Plus Syndrome(ID:disease_node_17741) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 5(ID:disease_node_16225) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dicer1 Syndrome(ID:disease_node_20090) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 100(ID:disease_node_16252) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 16(ID:disease_node_15310) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 6(ID:disease_node_14423) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1U(ID:disease_node_16887) (Disease)
Incoming r'ship SUBCLASS_OF to/from Culler-Jones Syndrome(ID:disease_node_20128) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cornelia De Lange Syndrome 1(ID:disease_node_19096) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 11A(ID:disease_node_18095) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental Dysplasia Of The Hip 2(ID:disease_node_15720) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 8(ID:disease_node_18946) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystransthyretinemic Hyperthyroxinemia(ID:disease_node_14391) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cryopyrin-Associated Periodic Syndromes(ID:disease_node_12214) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 79(ID:disease_node_16174) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1B(ID:disease_node_16899) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 10A(ID:disease_node_18093) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia(ID:disease_node_2724) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 47(ID:disease_node_16265) (Disease)
Incoming r'ship SUBCLASS_OF to/from Delta Beta-Thalassemia(ID:disease_node_15243) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 57(ID:disease_node_16239) (Disease)
Incoming r'ship SUBCLASS_OF to/from Duane-Radial Ray Syndrome(ID:disease_node_20157) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 30(ID:disease_node_16199) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 7(ID:disease_node_14299) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Arthrochalasia Type 1(ID:disease_node_18770) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Myopathy 1(ID:disease_node_18921) (Disease)
Incoming r'ship SUBCLASS_OF to/from Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1A(ID:disease_node_19119) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 91(ID:disease_node_16194) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dravet Syndrome(ID:disease_node_16267) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dysplastic Nevus Syndrome(ID:disease_node_2675) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 24(ID:disease_node_14338) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 67(ID:disease_node_16185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 104(ID:disease_node_16248) (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 33(ID:disease_node_16201) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 33(ID:disease_node_17270) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 64(ID:disease_node_16263) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nystagmus 3(ID:disease_node_20022) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 15 With Mandibulofacial Dysostosis(ID:disease_node_15309) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Aa(ID:disease_node_16914) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dentinogenesis Imperfecta(ID:disease_node_2440) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cornelia De Lange Syndrome 4(ID:disease_node_19093) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1D(ID:disease_node_16916) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 26(ID:disease_node_16203) (Disease)
Incoming r'ship SUBCLASS_OF to/from Early-Onset Dystonia And/Or Spastic Paraplegia(ID:disease_node_17262) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 4A(ID:disease_node_14279) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness Autosomal Domit 1(ID:disease_node_20051) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 54(ID:disease_node_16271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 59(ID:disease_node_16237) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1E(ID:disease_node_16909) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 20(ID:disease_node_15312) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Classic Type 2(ID:disease_node_18771) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 2B2(ID:disease_node_15787) (Disease)
Incoming r'ship SUBCLASS_OF to/from Domit Pericentral Pigmentary Retinopathy(ID:disease_node_15827) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 6B(ID:disease_node_16259) (Disease)
Incoming r'ship SUBCLASS_OF to/from Early-Onset Epilepsy 2(ID:disease_node_19680) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 16(ID:disease_node_18963) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 70(ID:disease_node_16182) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 2A(ID:disease_node_15785) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 69(ID:disease_node_16183) (Disease)
Incoming r'ship SUBCLASS_OF to/from D-2-Hydroxyglutaric Aciduria 2(ID:disease_node_16046) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 30(ID:disease_node_17273) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diffuse Cystic Renal Dysplasia(ID:disease_node_19891) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 41(ID:disease_node_16221) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Periodontal Type 2(ID:disease_node_18772) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 1A(ID:disease_node_14294) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 12(ID:disease_node_15315) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Kk(ID:disease_node_16897) (Disease)
Incoming r'ship SUBCLASS_OF to/from Duane Retraction Syndrome 3(ID:disease_node_20191) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 13(ID:disease_node_16218) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 97(ID:disease_node_16255) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Arthrochalasia Type 2(ID:disease_node_18769) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 66(ID:disease_node_16217) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 3(ID:disease_node_14424) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniosynostosis 6(ID:disease_node_19214) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness Autosomal Domit 3(ID:disease_node_20052) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia And Immunodeficiency 2(ID:disease_node_18090) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 21(ID:disease_node_14358) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Mm(ID:disease_node_16924) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 18(ID:disease_node_14274) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 4(ID:disease_node_16227) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ehlers-Danlos Syndrome Periodontal Type 1(ID:disease_node_18773) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dopa-Responsive Dystonia(ID:disease_node_14347) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 7(ID:disease_node_16202) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 2B1(ID:disease_node_15788) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 15(ID:disease_node_18964) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1C(ID:disease_node_16926) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 11(ID:disease_node_16268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 108(ID:disease_node_16244) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 3A(ID:disease_node_14291) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 25(ID:disease_node_17278) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 73(ID:disease_node_16179) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 18(ID:disease_node_15308) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myasthenic Syndrome 2A(ID:disease_node_14276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Early-Onset Epilepsy 3(ID:disease_node_19679) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniosynostosis 4(ID:disease_node_19210) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dehydrated Hereditary Stomatocytosis 2(ID:disease_node_15283) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 5(ID:disease_node_14426) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 1B(ID:disease_node_15782) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cortisone Reductase Deficiency 2(ID:disease_node_17242) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 93(ID:disease_node_16272) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 109(ID:disease_node_16260) (Disease)
Incoming r'ship SUBCLASS_OF to/from Duane Retraction Syndrome 1(ID:disease_node_20193) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 12(ID:disease_node_18096) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Symmetric Circumferential Skin Creases 1(ID:disease_node_19999) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cst3-Related Cerebral Amyloid Angiopathy(ID:disease_node_17494) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1S(ID:disease_node_16888) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1A(ID:disease_node_16917) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 19(ID:disease_node_16232) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 78(ID:disease_node_16175) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1R(ID:disease_node_16886) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 2(ID:disease_node_14427) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniosynostosis 2(ID:disease_node_19213) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 42(ID:disease_node_16210) (Disease)
Incoming r'ship SUBCLASS_OF to/from Desanto-Shinawi Syndrome(ID:disease_node_20081) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 62(ID:disease_node_16269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 9(ID:disease_node_17261) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1V(ID:disease_node_16915) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Myopathies(ID:disease_node_11395) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniosynostosis 1(ID:disease_node_19212) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 116(ID:disease_node_16242) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 31A(ID:disease_node_16226) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 92(ID:disease_node_16195) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolysis Bullosa Simplex Dowling-Meara Type(ID:disease_node_14236) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 46(ID:disease_node_16208) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 24(ID:disease_node_16234) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Symmetric Circumferential Skin Creases 2(ID:disease_node_19997) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diabetes Insipidus, Neurogenic(ID:disease_node_10720) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniosynostosis 3(ID:disease_node_19211) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 6(ID:disease_node_18956) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Cc(ID:disease_node_16918) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolysis Bullosa Simplex Ogna Type(ID:disease_node_14235) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Y(ID:disease_node_16885) (Disease)
Incoming r'ship SUBCLASS_OF to/from Denys-Drash Syndrome(ID:disease_node_11040) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 103(ID:disease_node_16249) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 13(ID:disease_node_15313) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Hh(ID:disease_node_16894) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 23(ID:disease_node_14339) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 14(ID:disease_node_16224) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness Autosomal Domit 2(ID:disease_node_20042) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Myopathy With Rimmed Vacuoles(ID:disease_node_18919) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Myopathy Tateyama Type(ID:disease_node_18915) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 8(ID:disease_node_14420) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 99(ID:disease_node_16253) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Jj(ID:disease_node_16904) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cornelia De Lange Syndrome 3(ID:disease_node_19094) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 27(ID:disease_node_16219) (Disease)
Incoming r'ship SUBCLASS_OF to/from Costello Syndrome(ID:disease_node_12240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dystonia 28, Childhood-Onset(ID:disease_node_17274) (Disease)
Incoming r'ship SUBCLASS_OF to/from Duane Retraction Syndrome 2(ID:disease_node_20192) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nystagmus 2(ID:disease_node_20023) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 58(ID:disease_node_16238) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2F(ID:disease_node_18857) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Dyserythropoietic Anemia Type Iiia(ID:disease_node_15272) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 32 Multiple Types(ID:disease_node_13708) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 4 Multiple Types(ID:disease_node_13701) (Disease)
Incoming r'ship SUBCLASS_OF to/from Complex Cortical Dysplasia With Other Brain Malformations(ID:disease_node_20057) (Disease)
Incoming r'ship SUBCLASS_OF to/from Central Conducting Lymphatic Anomaly(ID:disease_node_18242) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Muscular Dystrophy Due To Lmna Mutation(ID:disease_node_17428) (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 Type 2Y(ID:disease_node_18852) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2Dd(ID:disease_node_18865) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 6 Multiple Types(ID:disease_node_13706) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2A2A(ID:disease_node_18862) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 43(ID:disease_node_13674) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cardiofaciocutaneous Syndrome 3(ID:disease_node_19064) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 47(ID:disease_node_13698) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 1A(ID:disease_node_18872) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Dyserythropoietic Anemia Type Iva(ID:disease_node_15271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 29(ID:disease_node_13703) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2Z(ID:disease_node_18841) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cardiofaciocutaneous Syndrome 4(ID:disease_node_19063) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 5Q12 Deletion Syndrome(ID:disease_node_17101) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 15Q11.2 Deletion Syndrome(ID:disease_node_17113) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 17Q12 Deletion Syndrome(ID:disease_node_17107) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Fibrosis Of The Extraocular Muscles 3C(ID:disease_node_20097) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 19P13.13 Deletion Syndrome(ID:disease_node_17097) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 22 Multiple Types(ID:disease_node_13665) (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 Childhood-Onset Neurodegeneration With Brain Atrophy(ID:disease_node_16101) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2C(ID:disease_node_18840) (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 Chromosome 15Q25 Deletion Syndrome(ID:disease_node_17112) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 21 Multiple Types(ID:disease_node_13677) (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 Fibrosis Of The Extraocular Muscles 3A(ID:disease_node_20099) (Disease)
Incoming r'ship SUBCLASS_OF to/from Carpal Tunnel Syndrome 2(ID:disease_node_14253) (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 Cataract 5 Multiple Types(ID:disease_node_13678) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 42(ID:disease_node_13696) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Fibrosis Of The Extraocular Muscles 1(ID:disease_node_20101) (Disease)
Incoming r'ship SUBCLASS_OF to/from Carpal Tunnel Syndrome 1(ID:disease_node_14254) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 15 Multiple Types(ID:disease_node_13682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2D(ID:disease_node_18856) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2E(ID:disease_node_18855) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 20 Multiple Types(ID:disease_node_13693) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Limbs-Face Contractures-Hypotonia-Developmental Delay Syndrome(ID:disease_node_20091) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 2 Multiple Types(ID:disease_node_13700) (Disease)
Incoming r'ship SUBCLASS_OF to/from Common Variable Immunodeficiency 2(ID:disease_node_17327) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2V(ID:disease_node_18843) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Domit Intermediate F(ID:disease_node_18816) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2N(ID:disease_node_18844) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cone-Rod Dystrophy 24(ID:disease_node_16594) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2Q(ID:disease_node_18850) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Pituitary Hormone Deficiency 4(ID:disease_node_19694) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cardiofaciocutaneous Syndrome 2(ID:disease_node_19065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 12 Multiple Types(ID:disease_node_13694) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay(ID:disease_node_19995) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2O(ID:disease_node_18846) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 39 Multiple Types(ID:disease_node_13699) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 1B(ID:disease_node_18870) (Disease)
Incoming r'ship SUBCLASS_OF to/from Classical Lissencephalies And Subcortical Band Heterotopias(ID:disease_node_11895) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 33(ID:disease_node_13669) (Disease)
Incoming r'ship SUBCLASS_OF to/from Colorectal Neoplasms, Hereditary Nonpolyposis(ID:disease_node_2182) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Heart Defects, Dysmorphic Facial Features, And Intellectual Developmental Disorder(ID:disease_node_19996) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 1P36.33 Duplication Syndrome(ID:disease_node_19219) (Disease)
Incoming r'ship SUBCLASS_OF to/from Common Variable Immunodeficiency 13(ID:disease_node_17317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2J(ID:disease_node_18861) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 9 Multiple Types(ID:disease_node_13667) (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 Common Variable Immunodeficiency 10(ID:disease_node_17320) (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 Domit Intermediate E(ID:disease_node_18817) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cinca Syndrome(ID:disease_node_17360) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 1G(ID:disease_node_18868) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease, Axonal Type 2W(ID:disease_node_18858) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 2A1(ID:disease_node_18863) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 7(ID:disease_node_13673) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cardiofaciocutaneous Syndrome 1(ID:disease_node_19066) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 30(ID:disease_node_13685) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 1 Multiple Types(ID:disease_node_13704) (Disease)
Incoming r'ship SUBCLASS_OF to/from Common Variable Immunodeficiency 14(ID:disease_node_17316) (Disease)
Incoming r'ship SUBCLASS_OF to/from Central Precocious Puberty 1(ID:disease_node_17239) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Domit Intermediate G(ID:disease_node_18821) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Diarrhea 6(ID:disease_node_19332) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2Cc(ID:disease_node_18842) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 10 Multiple Types(ID:disease_node_13675) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Type 1E(ID:disease_node_18869) (Disease)
Incoming r'ship SUBCLASS_OF to/from Carney Complex(ID:disease_node_12272) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 41(ID:disease_node_13692) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 8 Multiple Types(ID:disease_node_13707) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 24(ID:disease_node_13676) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cleidocranial Dysplasia(ID:disease_node_2130) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 3 Multiple Types(ID:disease_node_13664) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 14 Multiple Types(ID:disease_node_13680) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 31 Multiple Types(ID:disease_node_13668) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2U(ID:disease_node_18848) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 16 Multiple Types(ID:disease_node_13683) (Disease)
Incoming r'ship SUBCLASS_OF to/from Central Precocious Puberty 2(ID:disease_node_17240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 13Q14 Deletion Syndrome(ID:disease_node_17115) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 11 Multiple Types(ID:disease_node_13684) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 37(ID:disease_node_13681) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease Axonal Type 2L(ID:disease_node_18847) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cherubism(ID:disease_node_2029) (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 Charcot-Marie-Tooth Disease Type 5(ID:disease_node_18814) (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 Or Isolated Pituitary Hormone Deficiency 8(ID:disease_node_19693) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Pituitary Hormone Deficiency 6(ID:disease_node_19689) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Megabladder(ID:disease_node_18268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Blepharophimosis-Impaired Intellectual Development Syndrome(ID:disease_node_20078) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 6(ID:disease_node_18048) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Isolated Macrothrombocytopenia 2(ID:disease_node_17051) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Severe Congenital Neutropenia(ID:disease_node_18061) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Progressive External Ophthalmoplegia 1(ID:disease_node_18046) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Spondyloepiphyseal Dysplasia Tarda(ID:disease_node_15691) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 4(ID:disease_node_18042) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Primary Microcephaly 27(ID:disease_node_19306) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Familial Infantile Seizures 6(ID:disease_node_16307) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Isolated Macrothrombocytopenia 1(ID:disease_node_17050) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bent Bone Dysplasia Syndrome 1(ID:disease_node_19037) (Disease)
Incoming r'ship SUBCLASS_OF to/from Baraitser-Winter Syndrome 1(ID:disease_node_20084) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Robinow Syndrome 3(ID:disease_node_17027) (Disease)
Incoming r'ship SUBCLASS_OF to/from Baraitser-Winter Syndrome 2(ID:disease_node_20082) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brain Small Vessel Disease 2(ID:disease_node_20011) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bronchiectasis 3(ID:disease_node_14714) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Wolfram Syndrome(ID:disease_node_20159) (Disease)
Incoming r'ship SUBCLASS_OF to/from Campomelic Dysplasia(ID:disease_node_12026) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Robinow Syndrome 1(ID:disease_node_17028) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brugada Syndrome 1(ID:disease_node_19138) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brachydactyly Type D(ID:disease_node_15751) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Familial Hematuria(ID:disease_node_18532) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Woolly Hair(ID:disease_node_17466) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brain Small Vessel Disease 1(ID:disease_node_20014) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bronchiectasis 1(ID:disease_node_14716) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques(ID:disease_node_19368) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Sideroblastic Anemia 4(ID:disease_node_15249) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bart-Pumphrey Syndrome(ID:disease_node_20167) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brugada Syndrome 9(ID:disease_node_19137) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cadasil 2(ID:disease_node_19912) (Disease)
Incoming r'ship SUBCLASS_OF to/from Branchio-Oto-Renal Syndrome(ID:disease_node_9904) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brooke-Spiegler Syndrome(ID:disease_node_20189) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Familial Infantile Seizures 2(ID:disease_node_16311) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 2(ID:disease_node_18050) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Primary Microcephaly 26(ID:disease_node_19307) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Familial Infantile Seizures 1(ID:disease_node_16312) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bosch-Boonstra-Schaaf Optic Atrophy Syndrome(ID:disease_node_20000) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Isolated Ectopia Lentis 1(ID:disease_node_13711) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bronchiectasis 2(ID:disease_node_14715) (Disease)
Incoming r'ship SUBCLASS_OF to/from Beare-Stevenson Cutis Gyrata Syndrome(ID:disease_node_20166) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Keratitis-Ichthyosis-Deafness Syndrome(ID:disease_node_20156) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 3(ID:disease_node_18047) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Thrombophilia Due To Protein S Deficiency(ID:disease_node_15584) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Robinow Syndrome 2(ID:disease_node_17029) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cadasil 1(ID:disease_node_19913) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Familial Infantile Seizures 5(ID:disease_node_16308) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Sensory Ataxia 1(ID:disease_node_16057) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brachial Plexus Neuritis(ID:disease_node_10872) (Disease)
Incoming r'ship SUBCLASS_OF to/from Birt-Hogg-Dube Syndrome(ID:disease_node_12487) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Limb-Girdle Muscular Dystrophy(ID:disease_node_18910) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bainbridge-Ropers Syndrome(ID:disease_node_20096) (Disease)
Incoming r'ship SUBCLASS_OF to/from Branchiooculofacial Syndrome(ID:disease_node_20190) (Disease)
Incoming r'ship SUBCLASS_OF to/from Benign Familial Infantile Seizures 3(ID:disease_node_16310) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 5(ID:disease_node_18049) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brachycephaly, Trichomegaly, And Developmental Delay(ID:disease_node_20134) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 8(ID:disease_node_16958) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Craniometaphyseal Dysplasia(ID:disease_node_19044) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Chondrodysplasia Punctata(ID:disease_node_19141) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3P Deletion Syndrome(ID:disease_node_17103) (Disease)
Incoming r'ship SUBCLASS_OF to/from Antithrombin Iii Deficiency(ID:disease_node_10120) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1B(ID:disease_node_18108) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Emery-Dreifuss Muscular Dystrophy 5(ID:disease_node_18880) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Heart Septal Defect 6(ID:disease_node_20071) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ankyrin-B-Related Cardiac Arrhythmia(ID:disease_node_20186) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 3(ID:disease_node_16962) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Standstill 1(ID:disease_node_20113) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Dyskeratosis Congenita 3(ID:disease_node_13637) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acrofacial Dysostosis Cincinnati Type(ID:disease_node_15740) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 3A(ID:disease_node_18099) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Heart Septal Defect 9(ID:disease_node_20065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 4(ID:disease_node_18107) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 10(ID:disease_node_15240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis 1(ID:disease_node_19128) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alzheimer'S Disease 2(ID:disease_node_16088) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autoimmune Lymphoproliferative Syndrome Type 4(ID:disease_node_13531) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3-Methylglutaconic Aciduria Type 7A(ID:disease_node_19197) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amyotrophic Lateral Sclerosis Type 26(ID:disease_node_14039) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Hypophosphatemic Rickets(ID:disease_node_19040) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alzheimer'S Disease 4(ID:disease_node_16083) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adult-Onset Leukoencephalopathy With Axonal Spheroids And Pigmented Glia(ID:disease_node_19919) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Heart Septal Defect 2(ID:disease_node_20075) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acrocephalosyndactylia(ID:disease_node_949) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autoinflammation, Antibody Deficiency, And Immune Dysregulation Syndrome(ID:disease_node_20132) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Alport Syndrome(ID:disease_node_19100) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aortic Valve Disease 3(ID:disease_node_20107) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acrokeratosis Verruciformis(ID:disease_node_19370) (Disease)
Incoming r'ship SUBCLASS_OF to/from App-Related Cerebral Amyloid Angiopathy(ID:disease_node_17493) (Disease)
Incoming r'ship SUBCLASS_OF to/from Advanced Sleep Phase Syndrome(ID:disease_node_15898) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Emery-Dreifuss Muscular Dystrophy 4(ID:disease_node_18881) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 9(ID:disease_node_16957) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Hypocalcemia(ID:disease_node_17543) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 10(ID:disease_node_16956) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adermatoglyphia(ID:disease_node_20038) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amyotrophic Lateral Sclerosis Type 25(ID:disease_node_14040) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alzheimer'S Disease 5(ID:disease_node_16086) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Craniodiaphyseal Dysplasia(ID:disease_node_19046) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aniridia 1(ID:disease_node_17297) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alzheimer'S Disease 1(ID:disease_node_16089) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acro-Osteolysis(ID:disease_node_11067) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 14(ID:disease_node_16963) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Heart Septal Defect 7(ID:disease_node_20070) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amyotrophic Lateral Sclerosis Type 28(ID:disease_node_14037) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 10(ID:disease_node_17352) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Congenital Deafness With Onychodystrophy(ID:disease_node_20102) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xx Sex Reversal 5(ID:disease_node_17164) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alexander Disease(ID:disease_node_11143) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 6(ID:disease_node_17159) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aortic Valve Disease 1(ID:disease_node_20109) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Beta Thalassemia(ID:disease_node_15246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alzheimer'S Disease 9(ID:disease_node_16071) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 12(ID:disease_node_16954) (Disease)
Incoming r'ship SUBCLASS_OF to/from Antley-Bixler Syndrome Without Disordered Steroidogenesis(ID:disease_node_13624) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis 3(ID:disease_node_19126) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 3(ID:disease_node_17157) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1A(ID:disease_node_18106) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Dyskeratosis Congenita 6(ID:disease_node_13632) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Distal Hereditary Motor Neuronopathy(ID:disease_node_18002) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 3B(ID:disease_node_18100) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 9(ID:disease_node_17158) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Dyskeratosis Congenita 1(ID:disease_node_13641) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aortic Valve Disease 2(ID:disease_node_20108) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Hyaline Body Myopathy(ID:disease_node_18941) (Disease)
Incoming r'ship SUBCLASS_OF to/from Andersen Syndrome(ID:disease_node_11420) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Dyskeratosis Congenita 4(ID:disease_node_13635) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ankylosing Spondylitis 2(ID:disease_node_17367) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Emery-Dreifuss Muscular Dystrophy 2(ID:disease_node_18883) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis 4(ID:disease_node_19125) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Aarskog Syndrome(ID:disease_node_20020) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adult Syndrome(ID:disease_node_20183) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Emery-Dreifuss Muscular Dystrophy 7(ID:disease_node_18878) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 8A(ID:disease_node_17354) (Disease)
Incoming r'ship SUBCLASS_OF to/from Angioedemas, Hereditary(ID:disease_node_11879) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alzheimer'S Disease 3(ID:disease_node_16081) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agammaglobulinemia 5(ID:disease_node_17349) (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 46,Xx Sex Reversal 4(ID:disease_node_17160) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Heart Septal Defect 5(ID:disease_node_20072) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Familial Visceral Neuropathy(ID:disease_node_19435) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 5(ID:disease_node_16960) (Disease)
Incoming r'ship SUBCLASS_OF to/from Atrial Heart Septal Defect 8(ID:disease_node_20069) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Dyskeratosis Congenita 2(ID:disease_node_13639) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amyotrophic Lateral Sclerosis Type 24(ID:disease_node_14041) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xx Sex Reversal 2(ID:disease_node_17161) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autoimmune Interstitial Lung, Joint, And Kidney Disease(ID:disease_node_14634) (Disease)
Incoming r'ship SUBCLASS_OF to/from Achondroplasia(ID:disease_node_920) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Cutis Laxa(ID:disease_node_17131) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 4(ID:disease_node_16961) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arrhythmogenic Right Ventricular Dysplasia 13(ID:disease_node_16953) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease)

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Autosomal Domit Disease

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