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Disease Ontology Browser
familial partial lipodystrophy type 1 (DOID:0070207)
Alliance: disease page
Synonyms: familial partial lipodystrophy Kobberling type; FPLD1
Alt IDs: OMIM:608600, MESH:D052496, ORDO:79084, UMLS_CUI:C1720859
Definition: A familial partial lipodystrophy characterized by loss of adipose tissue that is confined to the extremities with normal or increased fat in other areas of the body.


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
04/16/2024
MGI 6.23
The Jackson Laboratory