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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 FPLD, LIPE-related familial partial lipodystrophy, familial partial lipodystrophy associated with LIPE mutations,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee