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DOID:0070205 - familial partial lipodystrophy type 4
Disease Ontology Definition:A familial partial lipodystrophy characterized by autosomal dominant inheritance of loss of subcutaneous adipose tissue primarily from the lower limbs, insulin-resistant diabetes mellitus, hypertriglyceridemia, and hypertension that has_material_basis_in mutation in the PLIN1 gene on chromosome 15q26.
Synonyms: FPLD4, PLIN1-related FPLD, PLIN1-related familial partial lipodystrophy, familial partial lipodystrophy associated with PLIN1 mutations,
Xenbase Genes : plin1
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee