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Summary Literature (0)
DOID:0070206 - familial partial lipodystrophy type 6

Disease Ontology Definition:A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the LIPE gene on chromosome 19q13.

Synonyms: FPLD6, LIPE-related familial partial lipodystrophy, LIPE-related FPLD, familial partial lipodystrophy associated with LIPE mutations

Xenbase Genes : lipe


MIM:
MIM:615980 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6

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

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