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

Xenbase Genes : pparg, ppp1r3a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011448 - PPARG-related familial partial lipodystrophy


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

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