familial partial lipodystrophy type 3 (DOID:0070204)
Alliance: disease page
Synonyms: familial partial lipodystrophy associated with PPARG mutations; FPLD3; PPARG-related familial partial lipodystrophy; PPARG-related FPLD
Alt IDs: OMIM:604367, MESH:D052496, ORDO:79083, UMLS_CUI:C1720861
Definition: A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25.