ORPHA:79272
Sanfilippo syndrome type D
Also called GNS deficiency, Glucosamine N-acetyl-6-sulfatase deficiency, MPS3D, MPSIIID, Mucopolysaccharidosis type 3D, Mucopolysaccharidosis type IIID
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- 1-9 / 1 000 000 (Netherlands)
- Rarity class
- 1-9 / 1 000 000
ORPHA:79272 is classified under "Bone diseases" in the Orphanet nomenclature.