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Mucopolysaccharidosis type 4
rareA lysosomal storage disease belonging to the group of mucopolysaccharidoses, and characterized by spondylo-epiphyso-metaphyseal dysplasia. It exists in two forms, A and B.
- Identifiers
- MONDO:0018938 Orphanet:582
- Also known as
- eccentro-osteochondrodysplasia · eccentrochondrodysplasia · eccentroosteochondrodysplasia · Morquio disease · Morquio syndrome
Subtypes
| Disease | Subtypes |
|---|---|
| Morquio syndrome C | |
| Mucopolysaccharidosis type 4A | |
| Mucopolysaccharidosis type 4B |
Rare disease
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