Usher Syndrome Type 1G
Disease ID: disease_node_19179
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:606943 |
|---|---|
| Subclassof | DOID_0110826 |
| Data Source | DOID |
| Synonyms | USH1G, Usher syndrome type IG |
| Doid Label | Usher syndrome type 1G |
| Doid Description | An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19179 |
| Doid Id | DOID_0110834 |
| Label | Usher Syndrome Type 1G |
- Outgoing r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1(ID:disease_node_19175) (Disease)