Mucopolysaccharidosis type VII
Other Names for this Disease
- Beta-glucuronidase deficiency
- GUSB deficiency
- MPS 7
- MPS VII
- Mucopolysaccharidosis type 7
Your Questions Answeredby the Genetic and Rare Diseases Information Center
Please contact us with your questions about Mucopolysaccharidosis type VII. We will answer your question and update these pages with new resources and information.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.