Mucopolysaccharidosis type 7

Mucopolysaccharidosis type VII (MPS VII) is a very rare lysosomal storage disease belonging to the group of mucopolysaccharidoses.

Also known as: Beta-glucuronidase deficiency, MPS7, MPSVII, Mucopolysaccharidosis Type VII, Sly disease, Sly syndrome, beta-glucuronidase deficiency, mucopolysaccharidosis type 7

11 clinical trials for this condition and its sub-types, 8 tagged with Mucopolysaccharidosis type 7 itself.