ORPHA:582

Mucopolysaccharidosis type 4

Also called MPS4, MPSIV, Morquio disease, Mucopolysaccharidosis type IV

Body system

Bone diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Childhood, Infancy

Estimated prevalence

<1 / 1 000 000 (Sweden)

Rarity class

<1 / 1 000 000

ORPHA:582 is classified under "Bone diseases" in the Orphanet nomenclature.