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Disease Ontology Browser
familial partial lipodystrophy type 3 (DOID:0070204)
Alliance: disease page
Synonyms: familial partial lipodystrophy associated with PPARG mutations; FPLD3; PPARG-related familial partial lipodystrophy; PPARG-related FPLD
Alt IDs: OMIM:604367, MESH:D052496, ORDO:79083, UMLS_CUI:C1720861
Definition: A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.16
The Jackson Laboratory