| Term Name: | Usher syndrome type 3B |
|---|---|
| Synonyms: | USH3B, Usher syndrome type IIIB |
| Definition: | An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31. |
| Ontology: | Human Disease [DOID:0110842] ( DOID:0110842 ) |