ORPHA:309310
Mucopolysaccharidosis type 4B
Also called Beta-D-galactosidase deficiency, MPS4B, MPSIVB, Morquio disease type B, Mucopolysaccharidosis type IVB
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- <1 / 1 000 000 (United States)
- Rarity class
- <1 / 1 000 000
ORPHA:309310 is classified under "Bone diseases" in the Orphanet nomenclature.