ORPHA:67041

Hyaluronidase deficiency

Also called MPS9, MPSIX, Mucopolysaccharidosis type 9, Mucopolysaccharidosis type IX

Body system

Bone diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Childhood

Estimated prevalence

<1 / 1 000 000 (Europe)

Rarity class

<1 / 1 000 000

ORPHA:67041 is classified under "Bone diseases" in the Orphanet nomenclature.