Disease association ontology term - MONDO:0012071 - congenital generalized lipodystrophy type 1
Term summary
- ID
- MONDO:0012071
- Name
- congenital generalized lipodystrophy type 1
- Ontology or CV name
- Disease association
- Definition
- Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the AGPAT2 gene.
