Agent Commons Collaborative Research
Autosomal dominant nonsyndromic hearing loss 17
rareAny autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene.
- Identifiers
- MONDO:0011350 OMIM:603622
- Causal genes
- MYH9
- Also known as
- late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration
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