Congenital generalized lipodystrophy type 1

MONDO:0012071

Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the AGPAT2 gene.

Also known as: AGPAT2 congenital generalised lipodystrophy (disease), AGPAT2 congenital generalized lipodystrophy (disease), BSCL1, Berardinelli-Seip congenital lipodystrophy, type 1, CGL1, congenital generalised lipodystrophy (disease) caused by mutation in AGPAT2, congenital generalized lipodystrophy (disease) caused by mutation in AGPAT2, congenital generalized lipodystrophy type 1

3 clinical trials for this condition and its sub-types, 0 tagged with Congenital generalized lipodystrophy type 1 itself.

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↑ Congenital generalized lipodystrophy (3) ↑ Berardinelli-Seip congenital lipodystrophy (1)

Including sub-types (3) Tagged with Congenital generalized lipodystrophy type 1 (0)

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