Autosomal Genetic Disease

Disease ID: disease_node_15586

Connections displayed (default: 10).

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Subclassof	DOID_0050177
Data Source	DOID
Doid Label	autosomal genetic disease
Doid Description	A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
Disease Node Id	disease_node_15586
Doid Id	DOID_0050739
Label	Autosomal Genetic Disease

Incoming r'ship SUBCLASS_OF to/from Tubulinopathy(ID:disease_node_15780) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic Microphthalmia 12(ID:disease_node_16602) (Disease)
Incoming r'ship SUBCLASS_OF to/from Weill-Marchesani Syndrome(ID:disease_node_12336) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic Microphthalmia 14(ID:disease_node_16601) (Disease)
Incoming r'ship SUBCLASS_OF to/from Septo-Optic Dysplasia(ID:disease_node_10954) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 86(ID:disease_node_15794) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sotos Syndrome(ID:disease_node_12531) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spondylocostal Dysostosis 5(ID:disease_node_15608) (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 Hypophosphatasia(ID:disease_node_4200) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 30(ID:disease_node_16616) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Mediterranean Fever(ID:disease_node_6006) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fibrous Dysplasia, Polyostotic(ID:disease_node_3262) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Segmental Glomerulosclerosis 3(ID:disease_node_15759) (Disease)
Incoming r'ship SUBCLASS_OF to/from Factor Xi Deficiency(ID:disease_node_3148) (Disease)
Incoming r'ship SUBCLASS_OF to/from Distal Arthrogryposis Type 1C(ID:disease_node_15781) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dopamine Transporter Deficiency Syndrome(ID:disease_node_16696) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nystagmus 1(ID:disease_node_16615) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chromosome 1Q41-Q42 Deletion Syndrome(ID:disease_node_17025) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 55(ID:disease_node_16713) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Hemophilia A(ID:disease_node_15604) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Monogenic Disease(ID:disease_node_13650) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adenomatous Polyposis Coli(ID:disease_node_6248) (Disease)
Incoming r'ship SUBCLASS_OF to/from Aicardi-Goutieres Syndrome(ID:disease_node_17031) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)

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Autosomal Genetic Disease

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Disease Properties

Associated Connections 26

Disease Connections 26