Familial partial lipodystrophy associated with PPARG mutations

Disease ID:362
Name:Familial partial lipodystrophy associated with PPARG mutations
Associated with:1 target
Synonyms
Familial partial lipodystrophy | Lipodystrophy, familial partial, type 3; FPLD3
Database Links
Disease Ontology: DOID:0050440
OMIM: 604367
Orphanet: ORPHA79083

Targets

Peroxisome proliferator-activated receptor-γ

Ligands

No ligand related data available for Familial partial lipodystrophy associated with PPARG mutations