Syndrome

Disease ID: disease_node_7213

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Dbxref	MESH:D013577, NCI:C28193, SNOMEDCT_US_2023_03_01:64572001, UMLS_CUI:C0039082
Subclassof	DOID_4
Data Source	DOID, MESH
Mesh Id	D013577
Mesh Label	Syndrome
Mesh Subclassof	D004194
Doid Label	syndrome
Doid Description	A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality.
Disease Node Id	disease_node_7213
Doid Id	DOID_225
Label	Syndrome

Incoming r'ship SUBCLASS_OF to/from Ciliopathy(ID:disease_node_14682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zttk Syndrome(ID:disease_node_20153) (Disease)
Incoming r'ship SUBCLASS_OF to/from Xeroderma Pigmentosum(ID:disease_node_8034) (Disease)
Incoming r'ship SUBCLASS_OF to/from Yoon-Bellen Neurodevelopmental Syndrome(ID:disease_node_20313) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zaki Syndrome(ID:disease_node_20312) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zollinger-Ellison Syndrome(ID:disease_node_8058) (Disease)
Incoming r'ship SUBCLASS_OF to/from Yellow Nail Syndrome(ID:disease_node_12236) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zika Virus Congenital Syndrome(ID:disease_node_20310) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Retinitis Pigmentosa And Sinorespiratory Infections(ID:disease_node_13361) (Disease)
Incoming r'ship SUBCLASS_OF to/from Urinary Bladder, Overactive(ID:disease_node_11663) (Disease)
Incoming r'ship SUBCLASS_OF to/from Temple Syndrome(ID:disease_node_20246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sweeney-Cox Syndrome(ID:disease_node_20115) (Disease)
Incoming r'ship SUBCLASS_OF to/from Stolerman Neurodevelopmental Syndrome(ID:disease_node_20265) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tango2-Related Metabolic Encephalopathy And Arrythmias(ID:disease_node_20276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tetraamelia Syndrome(ID:disease_node_20228) (Disease)
Incoming r'ship SUBCLASS_OF to/from Teebi Hypertelorism Syndrome(ID:disease_node_20104) (Disease)
Incoming r'ship SUBCLASS_OF to/from Vissers-Bodmer Syndrome(ID:disease_node_20085) (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 Wolfram Syndrome(ID:disease_node_8007) (Disease)
Incoming r'ship SUBCLASS_OF to/from Williams Syndrome(ID:disease_node_9850) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wiskott-Aldrich Syndrome(ID:disease_node_7992) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wissler'S Syndrome(ID:disease_node_8001) (Disease)
Incoming r'ship SUBCLASS_OF to/from Weill-Marchesani Syndrome(ID:disease_node_12336) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torch Syndrome(ID:disease_node_20295) (Disease)
Incoming r'ship SUBCLASS_OF to/from Waisman Syndrome(ID:disease_node_20238) (Disease)
Incoming r'ship SUBCLASS_OF to/from Warsaw Breakage Syndrome(ID:disease_node_20331) (Disease)
Incoming r'ship SUBCLASS_OF to/from Subclavian Steal Syndrome(ID:disease_node_7149) (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 Vexas Syndrome(ID:disease_node_20296) (Disease)
Incoming r'ship SUBCLASS_OF to/from Stickler Syndrome(ID:disease_node_20111) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sudden Infant Death(ID:disease_node_7171) (Disease)
Incoming r'ship SUBCLASS_OF to/from Triple-A Syndrome(ID:disease_node_20363) (Disease)
Incoming r'ship SUBCLASS_OF to/from Tuberous Sclerosis(ID:disease_node_7665) (Disease)
Incoming r'ship SUBCLASS_OF to/from Trichorhinophalangeal Syndrome Type Iii(ID:disease_node_20114) (Disease)
Incoming r'ship SUBCLASS_OF to/from Reye Syndrome(ID:disease_node_6633) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ruijs-Aalfs Syndrome(ID:disease_node_20253) (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 Sotos Syndrome(ID:disease_node_12531) (Disease)
Incoming r'ship SUBCLASS_OF to/from Septo-Optic Dysplasia(ID:disease_node_10954) (Disease)
Incoming r'ship SUBCLASS_OF to/from Seckel Syndrome(ID:disease_node_20368) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schaaf-Yang Syndrome(ID:disease_node_20244) (Disease)
Incoming r'ship SUBCLASS_OF to/from Shwachman-Diamond Syndrome(ID:disease_node_498) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rhabdoid Tumor Predisposition Syndrome(ID:disease_node_20129) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rasopathy(ID:disease_node_19055) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schinzel Type Phocomelia(ID:disease_node_20232) (Disease)
Incoming r'ship SUBCLASS_OF to/from Salt And Pepper Syndrome(ID:disease_node_20352) (Disease)
Incoming r'ship SUBCLASS_OF to/from Shukla-Vernon Syndrome(ID:disease_node_20236) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia, Sensorineural Hearing Loss, Intellectual Developmental Disorder, And Leber Congenital Amaurosis(ID:disease_node_20227) (Disease)
Incoming r'ship SUBCLASS_OF to/from Renal Coloboma Syndrome(ID:disease_node_20077) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Intellectual Disability(ID:disease_node_20226) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rubinstein-Taybi Syndrome(ID:disease_node_6709) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short Stature, Hearing Loss, Retinitis Pigmentosa, And Distinctive Facies(ID:disease_node_20347) (Disease)
Incoming r'ship SUBCLASS_OF to/from Simpson-Golabi-Behmel Syndrome Type 2(ID:disease_node_20307) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sandestig-Stefanova Syndrome(ID:disease_node_20269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schwartz-Jampel Syndrome 1(ID:disease_node_20261) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sjogren-Larsson Syndrome(ID:disease_node_8580) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short Stature, Facial Dysmorphism, And Skeletal Anomalies With Or Without Cardiac Anomalies 2(ID:disease_node_20223) (Disease)
Incoming r'ship SUBCLASS_OF to/from Perrault Syndrome(ID:disease_node_20349) (Disease)
Incoming r'ship SUBCLASS_OF to/from Prader-Willi Syndrome(ID:disease_node_6283) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proximal Symphalangism(ID:disease_node_19033) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pcwh Syndrome(ID:disease_node_20080) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peters Plus Syndrome(ID:disease_node_20299) (Disease)
Incoming r'ship SUBCLASS_OF to/from Papa Syndrome(ID:disease_node_20116) (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 Persian Gulf Syndrome(ID:disease_node_9843) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pten Hamartoma Tumor Syndrome(ID:disease_node_20168) (Disease)
Incoming r'ship SUBCLASS_OF to/from Posterior Cervical Sympathetic Syndrome(ID:disease_node_12016) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pharc Syndrome(ID:disease_node_20309) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pseudo-Torch Syndrome 1(ID:disease_node_20356) (Disease)
Incoming r'ship SUBCLASS_OF to/from Progeroid Syndrome(ID:disease_node_19958) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pallister-Hall Syndrome(ID:disease_node_12001) (Disease)
Incoming r'ship SUBCLASS_OF to/from Post-Cardiac Arrest Syndrome(ID:disease_node_491) (Disease)
Incoming r'ship SUBCLASS_OF to/from Prune Belly Syndrome(ID:disease_node_6366) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pachyonychia Congenita(ID:disease_node_11715) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mulchandani-Bhoj-Conlin Syndrome(ID:disease_node_20245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteoarthropathy, Primary Hypertrophic(ID:disease_node_5757) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ogden Syndrome(ID:disease_node_19687) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteolysis, Essential(ID:disease_node_5772) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nijmegen Breakage Syndrome(ID:disease_node_11410) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodevelopmental Disorder With Hypotonia And Speech Delay(ID:disease_node_17040) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurooculocardiogenitourinary Syndrome(ID:disease_node_20019) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofacial Cleft(ID:disease_node_14023) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofaciodigital Syndromes(ID:disease_node_5739) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multicentric Reticulohistiocytosis(ID:disease_node_20222) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oculocerebrorenal Syndrome(ID:disease_node_5654) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mulibrey Nanism(ID:disease_node_11448) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Endocrine Neoplasia(ID:disease_node_5465) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephritis, Hereditary(ID:disease_node_5489) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Chemical Sensitivity(ID:disease_node_9769) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neonatal Lethal Pontocerebellar Hypoplasia, Hypotonia, And Respiratory Insufficiency Syndrome(ID:disease_node_20267) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nicolaides-Baraitser Syndrome(ID:disease_node_20079) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nail-Patella Syndrome(ID:disease_node_5399) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mls Syndrome(ID:disease_node_19243) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodevelopmental Disorder With Cataracts, Poor Growth, And Dysmorphic Facies(ID:disease_node_13713) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia And Hydranencephaly(ID:disease_node_20311) (Disease)
Incoming r'ship SUBCLASS_OF to/from Opitz Gbbb Syndrome(ID:disease_node_20283) (Disease)
Incoming r'ship SUBCLASS_OF to/from Marinesco-Sjogren Syndrome(ID:disease_node_20300) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lown-Ganong-Levine Syndrome(ID:disease_node_4842) (Disease)
Incoming r'ship SUBCLASS_OF to/from Midface Hypoplasia, Hearing Impairment, Elliptocytosis, And Nephrocalcinosis(ID:disease_node_20386) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Feil Syndrome(ID:disease_node_4529) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mednik Syndrome(ID:disease_node_20351) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kinsship Syndrome(ID:disease_node_19994) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lethal Congenital Contracture Syndrome(ID:disease_node_20327) (Disease)
Incoming r'ship SUBCLASS_OF to/from Median Arcuate Ligament Syndrome(ID:disease_node_286) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mayer-Rokitansky-Kuster-Hauser Syndrome(ID:disease_node_20233) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kleefstra Syndrome(ID:disease_node_17116) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mandibulofacial Dysostosis(ID:disease_node_4988) (Disease)
Incoming r'ship SUBCLASS_OF to/from Li-Fraumeni Syndrome(ID:disease_node_8936) (Disease)
Incoming r'ship SUBCLASS_OF to/from Maffucci Syndrome(ID:disease_node_20344) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Plus Disease(ID:disease_node_20241) (Disease)
Incoming r'ship SUBCLASS_OF to/from Koolen De Vries Syndrome(ID:disease_node_20165) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Trenaunay-Weber Syndrome(ID:disease_node_4532) (Disease)
Incoming r'ship SUBCLASS_OF to/from Loeys-Dietz Syndrome(ID:disease_node_12127) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microphthalmia With Limb Anomalies(ID:disease_node_20326) (Disease)
Incoming r'ship SUBCLASS_OF to/from Larsen-Like Syndrome B3Gat3 Type(ID:disease_node_20330) (Disease)
Incoming r'ship SUBCLASS_OF to/from Marsili Syndrome(ID:disease_node_15874) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mismatch Repair Cancer Syndrome(ID:disease_node_20231) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly-Micromelia Syndrome(ID:disease_node_20266) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meester-Loeys Syndrome(ID:disease_node_19688) (Disease)
Incoming r'ship SUBCLASS_OF to/from Langer-Giedion Syndrome(ID:disease_node_8482) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly And Chorioretinopathy 1(ID:disease_node_20317) (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 Ladd Syndrome(ID:disease_node_20093) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly And Chorioretinopathy 3(ID:disease_node_20314) (Disease)
Incoming r'ship SUBCLASS_OF to/from Laron Syndrome(ID:disease_node_11271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly And Chorioretinopathy 2(ID:disease_node_20315) (Disease)
Incoming r'ship SUBCLASS_OF to/from Laurence-Moon Syndrome(ID:disease_node_4594) (Disease)
Incoming r'ship SUBCLASS_OF to/from Linear Nevus Sebaceous Syndrome(ID:disease_node_20239) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mandibulofacial Dysostosis With Alopecia(ID:disease_node_20345) (Disease)
Incoming r'ship SUBCLASS_OF to/from Microcephaly, Growth Deficiency, Seizures, And Brain Malformations(ID:disease_node_20275) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile Liver Failure Syndrome(ID:disease_node_20281) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Arterial And Articular Multiple Calcification Syndrome(ID:disease_node_20247) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hermanski-Pudlak Syndrome(ID:disease_node_10905) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hengel-Maroofian-Schols Syndrome(ID:disease_node_20320) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intellectual Developmental Disorder With Short Stature And Behavioral Abnormalities(ID:disease_node_20237) (Disease)
Incoming r'ship SUBCLASS_OF to/from Juvenile Polyposis-Hereditary Hemorrhagic Telangiectasia Syndrome(ID:disease_node_20185) (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 Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome(ID:disease_node_20037) (Disease)
Incoming r'ship SUBCLASS_OF to/from High Myopia-Sensorineural Deafness Syndrome(ID:disease_node_20240) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypotonia, Ataxia, And Delayed Development Syndrome(ID:disease_node_20164) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypophosphatasia(ID:disease_node_4200) (Disease)
Incoming r'ship SUBCLASS_OF to/from Igsf1 Deficiency Syndrome(ID:disease_node_20251) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome(ID:disease_node_20256) (Disease)
Incoming r'ship SUBCLASS_OF to/from Image Syndrome(ID:disease_node_20348) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intellectual Developmental Disorder With Cardiac Arrhythmia(ID:disease_node_20280) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kagami-Ogata Syndrome(ID:disease_node_20385) (Disease)
Incoming r'ship SUBCLASS_OF to/from Intellectual Disability And Myopathy Syndrome(ID:disease_node_20316) (Disease)
Incoming r'ship SUBCLASS_OF to/from Holoprosencephaly(ID:disease_node_8636) (Disease)
Incoming r'ship SUBCLASS_OF to/from Histiocytosis-Lymphadenopathy Plus Syndrome(ID:disease_node_20252) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Alpha Tryptasemia Syndrome(ID:disease_node_19117) (Disease)
Incoming r'ship SUBCLASS_OF to/from Kenny-Caffey Syndrome(ID:disease_node_15651) (Disease)
Incoming r'ship SUBCLASS_OF to/from Growth Hormone Insensitivity Syndrome With Immune Dysregulation 1(ID:disease_node_20294) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ghosal Hematodiaphyseal Syndrome(ID:disease_node_20224) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fuchs' Heterochromic Uveitis(ID:disease_node_20198) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frasier Syndrome(ID:disease_node_11506) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hand-Foot-Genital Syndrome(ID:disease_node_20158) (Disease)
Incoming r'ship SUBCLASS_OF to/from Felty Syndrome(ID:disease_node_3206) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hallermann'S Syndrome(ID:disease_node_3645) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Encasement Syndrome(ID:disease_node_20324) (Disease)
Incoming r'ship SUBCLASS_OF to/from Halperin-Birk Syndrome(ID:disease_node_20319) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Dermal Hypoplasia(ID:disease_node_3276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fraser Syndrome(ID:disease_node_12538) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gapo Syndrome(ID:disease_node_20225) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fibromyalgia(ID:disease_node_3257) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fragile X Syndrome(ID:disease_node_3317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gamstorp-Wohlfart Syndrome(ID:disease_node_20383) (Disease)
Incoming r'ship SUBCLASS_OF to/from Goldenhar Syndrome(ID:disease_node_3556) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fibrogenesis Imperfecta Ossium(ID:disease_node_20308) (Disease)
Incoming r'ship SUBCLASS_OF to/from Harel-Yoon Syndrome(ID:disease_node_20086) (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 Fibrous Dysplasia, Polyostotic(ID:disease_node_3262) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fatigue Syndrome, Chronic(ID:disease_node_8414) (Disease)
Incoming r'ship SUBCLASS_OF to/from Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1(ID:disease_node_20322) (Disease)
Incoming r'ship SUBCLASS_OF to/from Culler-Jones Syndrome(ID:disease_node_20128) (Disease)
Incoming r'ship SUBCLASS_OF to/from Corpus Callosum Agenesis-Abnormal Genitalia Syndrome(ID:disease_node_19682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dysplastic Nevus Syndrome(ID:disease_node_2675) (Disease)
Incoming r'ship SUBCLASS_OF to/from Crest Syndrome(ID:disease_node_9279) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cryopyrin-Associated Periodic Syndromes(ID:disease_node_12214) (Disease)
Incoming r'ship SUBCLASS_OF to/from Denys-Drash Syndrome(ID:disease_node_11040) (Disease)
Incoming r'ship SUBCLASS_OF to/from Donohue Syndrome(ID:disease_node_12263) (Disease)
Incoming r'ship SUBCLASS_OF to/from Desanto-Shinawi Syndrome(ID:disease_node_20081) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diffuse Infiltrative Lymphocytosis Syndrome(ID:disease_node_20199) (Disease)
Incoming r'ship SUBCLASS_OF to/from Epidermolysis Bullosa Simplex With Muscular Dystrophy(ID:disease_node_20254) (Disease)
Incoming r'ship SUBCLASS_OF to/from De Lange Syndrome(ID:disease_node_2376) (Disease)
Incoming r'ship SUBCLASS_OF to/from Elsahy-Waters Syndrome(ID:disease_node_20298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniofacial Dysmorphism, Skeletal Anomalies, And Mental Retardation Syndrome(ID:disease_node_20272) (Disease)
Incoming r'ship SUBCLASS_OF to/from Duane-Radial Ray Syndrome(ID:disease_node_20157) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cri-Du-Chat Syndrome(ID:disease_node_2308) (Disease)
Incoming r'ship SUBCLASS_OF to/from Enchondromatosis(ID:disease_node_2903) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ellis-Van Creveld Syndrome(ID:disease_node_2761) (Disease)
Incoming r'ship SUBCLASS_OF to/from Deafness, Dystonia, And Cerebral Hypomyelination(ID:disease_node_13588) (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 Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 2(ID:disease_node_20321) (Disease)
Incoming r'ship SUBCLASS_OF to/from Endocrine-Cerebro-Osteodysplasia Syndrome(ID:disease_node_20325) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cystic Fibrosis(ID:disease_node_2353) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dicer1 Syndrome(ID:disease_node_20090) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dialysis Disequilibrium Syndrome(ID:disease_node_20318) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental Delay, Hypotrophy, And Dysmorphic Features Without Moebius Syndrome(ID:disease_node_20270) (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 Congenital Limbs-Face Contractures-Hypotonia-Developmental Delay Syndrome(ID:disease_node_20091) (Disease)
Incoming r'ship SUBCLASS_OF to/from Carey-Fineman-Ziter Syndrome(ID:disease_node_20301) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cauda Equina Syndrome(ID:disease_node_381) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charge Syndrome(ID:disease_node_12618) (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 Colorectal Neoplasms, Hereditary Nonpolyposis(ID:disease_node_2182) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cockayne Syndrome(ID:disease_node_2144) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Leptin Deficiency(ID:disease_node_20248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cerebellar Atrophy, Visual Impairment, And Psychomotor Retardation(ID:disease_node_20268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cerebellar Hyplasia/Atrophy, Epilepsy, And Global Developmental Delay(ID:disease_node_16534) (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 Autoimmune Interstitial Lung, Joint, And Kidney Disease(ID:disease_node_14634) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acquired Hyperostosis Syndrome(ID:disease_node_10068) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alopecia-Mental Retardation Syndrome(ID:disease_node_20302) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aicardi Syndrome(ID:disease_node_12576) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adie Syndrome(ID:disease_node_1003) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alkuraya-Kucinskas Syndrome(ID:disease_node_20384) (Disease)
Incoming r'ship SUBCLASS_OF to/from Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome(ID:disease_node_20297) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arc Syndrome(ID:disease_node_20360) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acrocallosal Syndrome(ID:disease_node_12106) (Disease)
Incoming r'ship SUBCLASS_OF to/from 3Mc Syndrome(ID:disease_node_20340) (Disease)
Incoming r'ship SUBCLASS_OF to/from Albinism, Oculocutaneous(ID:disease_node_8609) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amed Syndrome(ID:disease_node_19185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Antley-Bixler Syndrome With Disordered Steroidogenesis(ID:disease_node_13625) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aarskog Syndrome(ID:disease_node_20021) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aicardi-Goutieres Syndrome(ID:disease_node_17031) (Disease)
Incoming r'ship SUBCLASS_OF to/from Achondroplasia(ID:disease_node_920) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Spinal Artery Syndrome(ID:disease_node_10675) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alstrom Syndrome(ID:disease_node_12291) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adams-Oliver Syndrome(ID:disease_node_20339) (Disease)
Incoming r'ship SUBCLASS_OF to/from Angelman Syndrome(ID:disease_node_9087) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adult Syndrome(ID:disease_node_20183) (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 Brachycephaly, Trichomegaly, And Developmental Delay(ID:disease_node_20134) (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 Brachyolmia-Amelogenesis Imperfecta Syndrome(ID:disease_node_20255) (Disease)
Incoming r'ship SUBCLASS_OF to/from Baraitser-Winter Syndrome(ID:disease_node_20083) (Disease)
Incoming r'ship SUBCLASS_OF to/from Branchio-Oto-Renal Syndrome(ID:disease_node_9904) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bainbridge-Ropers Syndrome(ID:disease_node_20096) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bart-Pumphrey Syndrome(ID:disease_node_20167) (Disease)
Incoming r'ship SUBCLASS_OF to/from Basal Cell Nevus Syndrome(ID:disease_node_1494) (Disease)
Incoming r'ship SUBCLASS_OF to/from Branchiooculofacial Syndrome(ID:disease_node_20190) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bruck Syndrome(ID:disease_node_20338) (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 Bardet-Biedl Syndrome(ID:disease_node_10716) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bloom Syndrome(ID:disease_node_1624) (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 Beckwith-Wiedemann Syndrome(ID:disease_node_1504) (Disease)
Incoming r'ship SUBCLASS_OF to/from Breast Implant Illness(ID:disease_node_17660) (Disease)
Incoming r'ship SUBCLASS_OF to/from Coffin-Lowry Syndrome(ID:disease_node_11156) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chronic Atrial And Intestinal Dysrhythmia(ID:disease_node_20346) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chondrodysplasia Punctata(ID:disease_node_2065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cloves Syndrome(ID:disease_node_20306) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chediak-Higashi Syndrome(ID:disease_node_2023) (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 Carney Complex(ID:disease_node_12272) (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 Cleft Lip-Palate-Ectodermal Dysplasia Syndrome(ID:disease_node_20323) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cerebellofaciodental Syndrome(ID:disease_node_20271) (Disease)
Incoming r'ship SUBCLASS_OF to/from Caroli Syndrome(ID:disease_node_15475) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Disease(ID:disease_node_2554) (Disease)

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Disease Properties

Associated Connections 260

Disease Connections 260