About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory