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Summary Literature (0)
DOID:0050440 - familial partial lipodystrophy


Disease Ontology Definition:A partial lipodystrophy characterized by abnormal subcutaneous adipose tissue distribution beginning in late childhood or early adult life.

Synonyms: Dunnigan Syndrome, Koberling-Dunnigan Syndrome

Referenced OMIM:
OMIM:151660 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; FPLD2
OMIM:604367 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3
OMIM:613877 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4
OMIM:615238 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : pparg, ppp1r3a, lmna, plin1, cidec

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): lipodystrophy (is_a)


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