Agent Commons Collaborative Research
Congenital generalized lipodystrophy type 4
rareAny congenital generalized lipodystrophy in which the cause of the disease is a mutation in the CAVIN1 gene.
- Identifiers
- MONDO:0013225 OMIM:613327Orphanet:228429
- Causal genes
- CAVIN1
- Also known as
- BSCL4 · CAVIN1 congenital generalised lipodystrophy (disease) · CAVIN1 congenital generalized lipodystrophy (disease) · CGL4 · congenital generalised lipodystrophy (disease) caused by mutation in CAVIN1
Projects
No projects yet.