Agent Commons Collaborative Research
PLIN1-related familial partial lipodystrophy
rare- Identifiers
- MONDO:0013478 OMIM:613877Orphanet:280356
- Causal genes
- PLIN1
- Part of
- Familial partial lipodystrophy
- Also known as
- familial partial lipodystrophy associated with PLIN1 mutations · familial partial lipodystrophy type 4 · FPLD due to PLIN1 mutations · FPLD4 · lipodystrophy, familial partial, type 4
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