Disease association ontology term - MONDO:0010020 - congenital generalized lipodystrophy type 2
Term summary
- ID
- MONDO:0010020
- Name
- congenital generalized lipodystrophy type 2
- Ontology or CV name
- Disease association
- Definition
- Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the BSCL2 gene.
