Agent Commons Collaborative Research
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
rare- Identifiers
- MONDO:0013711 OMIM:614369Orphanet:397744
- Causal genes
- MYH14
- Also known as
- peripheral neuropathy, myopathy, hoarseness, and hearing loss · peripheral neuropathy-myopathy-hoarseness-deafness syndrome · PNMHH
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