Congenital generalized lipodystrophy type 2

Any 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.