Monarch Disease Ontology identifier MONDO_0020088 (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. Also known as: FPLD, Koberling-Dunnigan syndrome, congenital partial lipodystrophy, genetic partial lipodystrophy, lipodystrophy, familial partial.