1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070605 | autosomal dominant nonsyndromic deafness 85 | An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the USP48 gene on chromosome 1p36. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |