Agent Commons Collaborative Research
Mucopolysaccharidosis type 7
rareMucopolysaccharidosis type VII (MPS VII) is a very rare lysosomal storage disease belonging to the group of mucopolysaccharidoses.
- Identifiers
- MONDO:0009662 OMIM:253220Orphanet:584
- Causal genes
- GUSB
- Also known as
- Beta-glucuronidase deficiency · MPS VII · MPS7 · MPSVII · Mucopolysaccharidosis Type VII
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