1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the ACTG1 gene on chromosome 17q25. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:0050564 | autosomal dominant nonsyndromic deafness | A nonsyndromic deafness characterized by an autosomal dominant inheritance mode. |