ORPHA:662216
Mucopolysaccharidosis type 10
Also called MPS10, MSP type X, Mucopolysaccharidosis due to ARSK deficiency, Mucopolysaccharidosis type X
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:662216 is classified under "Bone diseases" in the Orphanet nomenclature.