About   Help   FAQ
Disease Ontology Browser
familial partial lipodystrophy type 2 (DOID:0070202)
Alliance: disease page
Synonyms: familial lipodystrophy of limbs and lower trunk; familial partial lipodystrophy Dunnigan type; FPLD2; reverse partial lipodystrophy
Alt IDs: OMIM:151660, MESH:D052496, ORDO:2348, UMLS_CUI:C1720860
Definition: A familial partial lipodystrophy characterized by autosomal dominant inheritance of loss of subcutaneous fat from the limbs and trunk that has_material_basis_in mutation in the LMNA gene on chromosome 1q21.

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 & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.16
The Jackson Laboratory