Autosomal recessive limb-girdle muscular dystrophy type 2U

Any autosomal recessive limb-girdle muscular dystrophy in which the cause of the disease is a mutation in the ISPD gene.

Also known as: ISPD autosomal recessive limb-girdle muscular dystrophy, LGMD2U, MDDGC7, autosomal recessive limb-girdle muscular dystrophy caused by mutation in ISPD, muscular dystrophy, limb-girdle, type 2U, muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7

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