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CIDEC-related familial partial lipodystrophy

MONDO:0014098

Also known as: CIDEC-related FPLD, CIDEC-related familial partial lipodystrophy, FPLD5, lipodystrophy, familial partial, associated with Cidec mutations, lipodystrophy, familial partial, type 5

4 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Skin disorder (132) Inborn errors of metabolism (45) Lipodystrophy (27) Human disease (14) Familial partial lipodystrophy (11) Partial lipodystrophy (7) Hereditary skin disorder (6)

Trials to join now! 3 Completed 1

Rare fat disorder gene hunt: just 2 patients could unlock answers

Knowledge-focused Completed

This study looked for a new gene that causes hereditary lipodystrophy, a rare disease where people lose body fat and often develop diabetes and heart problems. Researchers studied DNA and cells from 2 patients who had the disease but no known genetic cause. The goal was to find t…

Phase: NA • Sponsor: University Hospital, Bordeaux • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:00 UTC