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Disease Ontology Browser
familial partial lipodystrophy type 6 (DOID:0070206)
Alliance: disease page
Synonyms: familial partial lipodystrophy associated with LIPE mutations; FPLD6; LIPE-related familial partial lipodystrophy; LIPE-related FPLD
Alt IDs: OMIM:615980, ORDO:435660
Definition: A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the LIPE gene on chromosome 19q13.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory