Usher Syndrome Type 1D
Disease ID: disease_node_19182
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:601067 |
|---|---|
| Subclassof | DOID_0110826, DOID_0080578 |
| Data Source | DOID |
| Synonyms | USH1D, Usher syndrome type ID |
| Doid Label | Usher syndrome type 1D |
| Doid Description | An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22. |
| Has Material Basis In | GENO_0000148, GENO_0000930 |
| Disease Node Id | disease_node_19182 |
| Doid Id | DOID_0110831 |
| Label | Usher Syndrome Type 1D |
- Outgoing r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1(ID:disease_node_19175) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Digenic Disease(ID:disease_node_13627) (Disease)