Usher Syndrome Type 1C
Disease ID: disease_node_19183
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:276904 |
|---|---|
| Subclassof | DOID_0110826 |
| Data Source | DOID |
| Synonyms | USH1C, Usher syndrome type I Acadian variety, Usher syndrome type IC |
| Doid Label | Usher syndrome type 1C |
| Doid Description | An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19183 |
| Doid Id | DOID_0110830 |
| Label | Usher Syndrome Type 1C |
- Outgoing r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1(ID:disease_node_19175) (Disease)