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Congenital generalized lipodystrophy type 2
MONDO:0010020Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the BSCL2 gene.
Also known as: BSCL2 congenital generalised lipodystrophy (disease), BSCL2 congenital generalized lipodystrophy (disease), CGL2, congenital generalised lipodystrophy (disease) caused by mutation in BSCL2, congenital generalized lipodystrophy (disease) caused by mutation in BSCL2, BSCL2-related Brunzell syndrome, Berardinelli Seip congenital lipodystrophy type 2, Berardinelli syndrome
3 clinical trials for this condition and its sub-types, 0 tagged with Congenital generalized lipodystrophy type 2 itself.
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