Wolfram Syndrome
Disease ID: disease_node_8007
Connections displayed (default: 10).
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| Dbxref | GARD:7898, MESH:D014929, NCI:C35133, ORDO:3463, SNOMEDCT_US_2023_03_01:70694009, UMLS_CUI:C0043207 |
|---|---|
| Subclassof | DOID_225 |
| Data Source | DOID, MESH |
| Synonyms | WFS |
| Mesh Id | D014929 |
| Mesh Label | Wolfram Syndrome |
| Mesh Subclassof | D003919, D003922, D054062, D015418 |
| Doid Label | Wolfram syndrome |
| Doid Description | A syndrome that is characterized by diabetes mellitus, optic atrophy, and deafness. OMIM mapping confirmed by DO. [LS]. |
| Disease Node Id | disease_node_8007 |
| Doid Id | DOID_10632 |
| Label | Wolfram Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Wolfram Syndrome 1(ID:disease_node_20160) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Autosomal Domit Wolfram Syndrome(ID:disease_node_20159) (Disease)