Physical Disorder

Disease ID: disease_node_13159

Connections displayed (default: 10).

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Subclassof	DOID_4
Data Source	DOID
Synonyms	congenital disorder
Doid Label	physical disorder
Doid Description	A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment.
Disease Node Id	disease_node_13159
Doid Id	DOID_0080015
Label	Physical Disorder

Incoming r'ship SUBCLASS_OF to/from Linear Skin Defects With Multiple Congenital Anomalies 2(ID:disease_node_19244) (Disease)
Incoming r'ship SUBCLASS_OF to/from Zika Virus Congenital Syndrome(ID:disease_node_20310) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy(ID:disease_node_19897) (Disease)
Incoming r'ship SUBCLASS_OF to/from Toxoplasmosis, Congenital(ID:disease_node_7507) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syphilis, Congenital(ID:disease_node_7234) (Disease)
Incoming r'ship SUBCLASS_OF to/from Torch Syndrome(ID:disease_node_20295) (Disease)
Incoming r'ship SUBCLASS_OF to/from Rapidly Involuting Congenital Hemangioma(ID:disease_node_20680) (Disease)
Incoming r'ship SUBCLASS_OF to/from Severe Congenital Neutropenia(ID:disease_node_18054) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations(ID:disease_node_15686) (Disease)
Incoming r'ship SUBCLASS_OF to/from Silver-Russell Syndrome(ID:disease_node_12257) (Disease)
Incoming r'ship SUBCLASS_OF to/from Poland Syndrome(ID:disease_node_6215) (Disease)
Incoming r'ship SUBCLASS_OF to/from Polydactyly(ID:disease_node_9293) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Congenital Glaucoma(ID:disease_node_14333) (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 Myasthenic Syndromes, Congenital(ID:disease_node_10478) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Congenital Cyst Of Kidney(ID:disease_node_13259) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nonsyndromic Congenital Nail Disorder(ID:disease_node_18446) (Disease)
Incoming r'ship SUBCLASS_OF to/from Orofacial Cleft(ID:disease_node_14023) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephroma, Mesoblastic(ID:disease_node_9395) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neural Tube Defect(ID:disease_node_20731) (Disease)
Incoming r'ship SUBCLASS_OF to/from Myotonia Congenita(ID:disease_node_5387) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nystagmus, Congenital(ID:disease_node_10580) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neonatal Diabetes Mellitus With Congenital Hypothyroidism(ID:disease_node_17246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome(ID:disease_node_16969) (Disease)
Incoming r'ship SUBCLASS_OF to/from Laryngomalacia(ID:disease_node_12041;disease_node_20772) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis(ID:disease_node_12393) (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 Anemia, Hemolytic, Congenital(ID:disease_node_1187) (Disease)
Incoming r'ship SUBCLASS_OF to/from Arthrogryposis Multiplex Congenita(ID:disease_node_20565) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anus, Imperforate(ID:disease_node_1287) (Disease)
Incoming r'ship SUBCLASS_OF to/from Afibrinogenemia(ID:disease_node_1054) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anemia, Hypoplastic, Congenital(ID:disease_node_11024) (Disease)
Incoming r'ship SUBCLASS_OF to/from Blepharophimosis(ID:disease_node_8800) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex(ID:disease_node_18269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Caudal Regression Syndrome(ID:disease_node_20771) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Hereditary Endothelial Dystrophy Of Cornea(ID:disease_node_17120) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Bilateral Absence Of Vas Deferens(ID:disease_node_17151) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Muscular Dystrophy(ID:disease_node_17393) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorders Of Glycosylation(ID:disease_node_9854) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Leptin Deficiency(ID:disease_node_20248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Granular Cell Tumor(ID:disease_node_17884) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Aphakia(ID:disease_node_13710) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Generalized Lipodystrophy(ID:disease_node_20148) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Intrinsic Factor Deficiency(ID:disease_node_17077) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Hypothyroidism(ID:disease_node_2303) (Disease)
Incoming r'ship SUBCLASS_OF to/from Compton-North Congenital Myopathy(ID:disease_node_18960) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Adrenal Insufficiency(ID:disease_node_17794) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Adrenal Hyperplasia(ID:disease_node_16839) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Mirror Movement Disorder(ID:disease_node_16708) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Hypotrichosis With Juvenile Macular Dystrophy(ID:disease_node_14196) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Fibrosarcoma(ID:disease_node_17986) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Megabladder(ID:disease_node_18268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Hypogammaglobulinemia(ID:disease_node_17345) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Bile Acid Synthesis Defect(ID:disease_node_16836) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Chylothorax(ID:disease_node_18331) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Diarrhea(ID:disease_node_19331) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental Cardiac Valvular Defect(ID:disease_node_20773) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Secretory Sodium Diarrhea 3(ID:disease_node_19341) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Ptosis(ID:disease_node_20774) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nervous System Abnormality(ID:disease_node_13582) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Myopathy 4A(ID:disease_node_18958) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cryptophthalmia(ID:disease_node_20767) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Secretory Sodium Diarrhea 8(ID:disease_node_19342) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gastroschisis(ID:disease_node_10075) (Disease)
Incoming r'ship SUBCLASS_OF to/from Heart Defects, Congenital(ID:disease_node_3719) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gingival Neoplasms(ID:disease_node_3462) (Disease)
Incoming r'ship SUBCLASS_OF to/from Flatfoot(ID:disease_node_3269) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hernia, Diaphragmatic(ID:disease_node_3936) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hernia, Umbilical(ID:disease_node_3943) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypospadias(ID:disease_node_4216) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ichthyosis, Lamellar(ID:disease_node_9185) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meckel Diverticulum(ID:disease_node_5047) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lethal Congenital Contracture Syndrome(ID:disease_node_20327) (Disease)
Incoming r'ship SUBCLASS_OF to/from Klippel-Feil Syndrome(ID:disease_node_4529) (Disease)
Incoming r'ship SUBCLASS_OF to/from Linear Skin Defects With Multiple Congenital Anomalies 3(ID:disease_node_19245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lethal Congenital Glycogen Storage Disease Of Heart(ID:disease_node_20393) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Disease(ID:disease_node_2554) (Disease)

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Physical Disorder

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Disease Properties

Associated Connections 77

Disease Connections 77