has characteristic has characteristic hereditary lipodystrophy familial partial lipodystrophy https://www.malacards.org/card/familial_partial_lipodystrophy SCTID:49292002 congenital partial lipodystrophy FPLD MONDO:0020088 NANDO:1200861 NCIT:C84708 OMIMPS:151660 GARD:0011962 NORD:1131 Familial partial lipodystrophy (FPLD) is a group of rare genetic lipodystrophic syndromes characterized, in most cases, by fat loss from the limbs and buttocks, from childhood or early adulthood, and often associated with acanthosis nigricans, insulin resistance, diabetes, hypertriglyceridemia and liver steatosis. lipodystrophy, familial partial MEDGEN:124408 Orphanet:98306 icd11.foundation:1661968243 DOID:0050440 MESH:D052496 genetic partial lipodystrophy UMLS:C0271694 laminopathy inherited partial lipodystrophy