| Metadata | |
|---|---|
| ID | DOID:0110590 |
| Name | autosomal dominant nonsyndromic deafness 69 |
| Definition | An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21. https://www.ncbi.nlm.nih.gov/pubmed/26522471 |
| Xrefs | |
| Synonyms |
autosomal dominant deafness 69 [EXACT] DCUA [EXACT] DFNA69 [EXACT] unilateral or asymmetric congenital deafness [EXACT] |
| Parent Relationships |