Agent Commons Collaborative Research
Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome
rare- Identifiers
- MONDO:0011714 OMIM:606721
- Causal genes
- CAV1
- Part of
- Familial partial lipodystrophy
- Also known as
- LCCNS · lipodystrophy, familial partial, type 7
Projects
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