Usher Syndrome Type 1J
Disease ID: disease_node_19177
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H35.5, MIM:614869 |
|---|---|
| Subclassof | DOID_0110826 |
| Data Source | DOID |
| Synonyms | USH1J, Usher syndrome type IJ |
| Doid Label | Usher syndrome type 1J |
| Doid Description | An Usher syndrome type 1 that has_material_basis_in caused by homozygous mutation in the CIB2 gene on chromosome 15q24. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19177 |
| Doid Id | DOID_0110836 |
| Label | Usher Syndrome Type 1J |
- Outgoing r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1(ID:disease_node_19175) (Disease)