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Summary Literature (0)
DOID:0070204 - familial partial lipodystrophy type 3


Disease Ontology Definition:A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25.

Synonyms: FPLD3, PPARG-related FPLD, PPARG-related familial partial lipodystrophy, familial partial lipodystrophy associated with PPARG mutations

Referenced OMIM:
OMIM:604367 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3

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

Xenbase Genes : pparg, ppp1r3a

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), familial partial lipodystrophy (is_a)


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