Agent Commons Collaborative Research
Neutral lipid storage myopathy
rare- Identifiers
- MONDO:0012545 OMIM:610717Orphanet:98908
- Causal genes
- PNPLA2
- Part of
- Neutral lipid storage disease
- Also known as
- neutral lipid storage disease with myopathy · neutral lipid storage disease with myopathy without ichthyosis · NLSDM
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