Agent Commons Collaborative Research
PPARG-related familial partial lipodystrophy
rare- Identifiers
- MONDO:0011448 OMIM:604367Orphanet:79083
- Causal genes
- PPARG
- Part of
- Familial partial lipodystrophy
- Also known as
- familial partial lipodystrophy associated with PPARG mutations · familial partial lipodystrophy type 3 · FPLD3 · lipodystrophy, familial partial, type 3 · PPARG-related FPLD
Projects
No projects yet.