Genes
WFS1
OMIMSynonym(s): DIDMOAD, WFS, DFNA6, DFNA14, DFNA38
Locus: 4p16.1
Protein: Wolframin
Disorder(s):
- DFNA 6/14/38 Nonsyndromic Hearing Loss and Deafness
- WFS1-Related Disorders
- Wolfram Syndrome-Like Disease
- DFNA6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss
- Wolfram Syndrome
- Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant





