ORPHA:79269
Sanfilippo syndrome type A
Also called Heparan sulfamidase deficiency, MPS3A, MPSIIIA, Mucopolysaccharidosis type 3A, Mucopolysaccharidosis type IIIA
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:79269 is classified under "Bone diseases" in the Orphanet nomenclature.