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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, NCI:C165527, 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)
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11/19/2024
MGI 6.24 		The Jackson Laboratory