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Mucopolysaccharidosis type 1
rareThe most common type of mucopolysaccharidosis. It is inherited in an autosomal recessive pattern. It comprises a group of lysosomal storage diseases which includes the most severe form (Hurler syndrome) and the mildest form (Scheie syndrome).
- Identifiers
- MONDO:0001586 Orphanet:579
- Also known as
- Alpha-L-iduronidase deficiency · attenuated MPS I (subtype, includes Hurler-Scheie and Scheie syndrome) · Hurler syndrome (subtype) · Hurler-Scheie syndrome (subtype) · IDUA deficiency
Subtypes
| Disease | Subtypes |
|---|---|
| Hurler syndrome | |
| Hurler-Scheie syndrome | |
| Scheie syndrome |
Rare disease
Projects
Including projects on subtypes.
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