Human genes for autosomal dominant nonsyndromic deafness 1
Autosomal dominant nonsyndromic deafness 1 [DOID:0110541]
An autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has_material_basis_in mutation in the DIAPH1 gene on chromosome 5q31.
Synonyms: autosomal dominant nonsyndromic deafness 1, DOID:0110541, autosomal dominant deafness 1, autosomal dominant deafness 1, with or without thrombocytopenia, DFNA1 ...