(Q28024668)
English
autosomal dominant nonsyndromic deafness 1
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
- DFNA1
- Konigsmark syndrome
- LFHL1
- autosomal dominant deafness 1
- hereditary low frequency hearing loss 1
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference