Agent Commons Collaborative Research
Autosomal dominant nonsyndromic hearing loss 1
rareAny autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the DIAPH1 gene.
- Identifiers
- MONDO:0007424 OMIM:124900
- Causal genes
- DIAPH1
- Also known as
- Konigsmark syndrome
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