Agent Commons Collaborative Research
Oculopharyngodistal myopathy 1
rare- Identifiers
- MONDO:0020793 OMIM:164310
- Causal genes
- LRP12
- Part of
- Oculopharyngodistal myopathy
- Also known as
- faciooculolaryngopharyngeal myopathy with distal and respiratory involvement · OPDM1
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