Wolfram Syndrome 1
Disease ID: disease_node_20160
Connections displayed (default: 10).
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| Dbxref | ICD10CM:E13.8, MIM:222300 |
|---|---|
| Subclassof | DOID_0050737, DOID_10632 |
| Data Source | DOID |
| Synonyms | DIDMOAD, WFS1, diabetes mellitus AND insipidus with optic atrophy AND deafness |
| Doid Label | Wolfram syndrome 1 |
| Doid Description | An autosomal recessive disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the WFS1 gene on chromosome 4p16.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20160 |
| Doid Id | DOID_0110629 |
| Label | Wolfram Syndrome 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Wolfram Syndrome(ID:disease_node_8007) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)