Usher Syndrome Type 1F
Disease ID: disease_node_19181
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:602083 |
|---|---|
| Subclassof | DOID_0110826 |
| Data Source | DOID |
| Synonyms | USH1F, Usher syndrome type IF |
| Doid Label | Usher syndrome type 1F |
| Doid Description | An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19181 |
| Doid Id | DOID_0110832 |
| Label | Usher Syndrome Type 1F |
- Outgoing r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1(ID:disease_node_19175) (Disease)