autosomal recessive nonsyndromic deafness 30
MeSH: C564624ORPHA: 90636
Overview
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutations in the MYO3A gene on chromosome 10p12.1
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C564624Orphanet Code
ORPHA:90636autosomal recessive nonsyndromic deafness 30
| MeSH | C564624 |
| Orphanet | ORPHA:90636 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO