Disease

Familial Partial Lipodystrophy

About the Disease
Familial Partial Lipodystrophy, also known as lipodystrophy, familial partial, is related to lipodystrophy, familial partial, type 1 and lipodystrophy, familial partial, type 6, and has symptoms including myalgia An important gene associated with Familial Partial Lipodystrophy is LMNA (Lamin A/C), and among its related pathways/superpathways are Metabolism and Signal Transduction. The drugs Chenodeoxycholic acid and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include skin, liver and pancreas, and related phenotypes are no effect and no effect

Common Targets
ANGPTL3 | PPARG | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | APOC3 | LEPR | PNPLA2 | LMNA | PLIN1 | LIPE | POLD1

疾病靶点研报
Familial Partial Lipodystrophy

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