Digenic Disease

Disease ID: disease_node_13627

Connections displayed (default: 10).

Plants :

Formulations :

Phytochemicals :

Other Diseases :

Loading graph...

ℹ️ Click here to know more about the properties

Subclassof	DOID_0080577
Data Source	DOID
Doid Label	digenic disease
Doid Description	A polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes.
Disease Node Id	disease_node_13627
Doid Id	DOID_0080578
Label	Digenic Disease

Incoming r'ship SUBCLASS_OF to/from Usher Syndrome Type 2C(ID:disease_node_19170) (Disease)
Incoming r'ship SUBCLASS_OF to/from Usher Syndrome Type 1D(ID:disease_node_19182) (Disease)
Incoming r'ship SUBCLASS_OF to/from Spinocerebellar Ataxia Type 17(ID:disease_node_15996) (Disease)
Incoming r'ship SUBCLASS_OF to/from Short-Rib Thoracic Dysplasia 7 With Or Without Polydactyly(ID:disease_node_15730) (Disease)
Incoming r'ship SUBCLASS_OF to/from Parkinson'S Disease 6(ID:disease_node_16132) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteasome-Associated Autoinflammatory Syndrome 3(ID:disease_node_15596) (Disease)
Incoming r'ship SUBCLASS_OF to/from Proteasome-Associated Autoinflammatory Syndrome 1(ID:disease_node_15599) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Pulmonary Hypertension(ID:disease_node_13642) (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 Methylmalonic Aciduria And Homocystinuria Type Cblc(ID:disease_node_19192) (Disease)
Incoming r'ship SUBCLASS_OF to/from Long Qt Syndrome 1(ID:disease_node_16880) (Disease)
Incoming r'ship SUBCLASS_OF to/from Joubert Syndrome 15(ID:disease_node_14702) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Hypophosphatemic Rickets With Hypercalciuria(ID:disease_node_19041) (Disease)
Incoming r'ship SUBCLASS_OF to/from Facioscapulohumeral Muscular Dystrophy 2(ID:disease_node_18874) (Disease)
Incoming r'ship SUBCLASS_OF to/from Facioscapulohumeral Muscular Dystrophy 4(ID:disease_node_18876) (Disease)
Incoming r'ship SUBCLASS_OF to/from Facioscapulohumeral Muscular Dystrophy 3(ID:disease_node_18877) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dyskeratosis Congenita(ID:disease_node_10031) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Polygenic Disease(ID:disease_node_17150) (Disease)
Incoming r'ship SUBCLASS_OF to/from Coproporphyria, Hereditary(ID:disease_node_11282) (Disease)
Incoming r'ship SUBCLASS_OF to/from Craniosynostosis 7(ID:disease_node_13626) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal-Mitochondrial Sensorineural Deafness(ID:disease_node_17739) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Recessive Nonsyndromic Deafness 1A(ID:disease_node_15040) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acrocallosal Syndrome(ID:disease_node_12106) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amed Syndrome(ID:disease_node_19185) (Disease)

Back to Browse Back to Home

GRAYU Website

Grayu

Digenic Disease

Graph

Disease Properties

Associated Connections 24

Disease Connections 24