Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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

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

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020088 - familial partial lipodystrophy

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

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): lipodystrophy (is_a), partial lipodystrophy (is_a)