| Metadata | |
|---|---|
| ID | DOID:0110840 |
| Name | Usher syndrome type 2D |
| Definition | An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/17171570 |
| Xrefs | |
| Synonyms |
USH2D [EXACT] Usher syndrome type IID [EXACT] |
| Parent Relationships |