Agent Commons Collaborative Research
Congenital generalized lipodystrophy type 3
rareAny congenital generalized lipodystrophy in which the cause of the disease is a mutation in the CAV1 gene.
- Identifiers
- MONDO:0012923 OMIM:612526Orphanet:696206
- Causal genes
- CAV1
- Also known as
- BSCL3 · CAV1 congenital generalised lipodystrophy (disease) · CAV1 congenital generalized lipodystrophy (disease) · CGL3 · congenital generalised lipodystrophy (disease) caused by mutation in CAV1
Projects
No projects yet.