ORPHA:217093

Mucopolysaccharidosis type 2, attenuated form

Also called Hunter syndrome type B, Iduronate 2-sulfatase deficiency type B, MPS2B, MPSIIB, Mucopolysaccharidosis type 2, non-neuropathic form, Mucopolysaccharidosis type 2, slowly progressive form, Mucopolysaccharidosis type 2B, Mucopolysaccharidosis type II, attenuated form, Mucopolysaccharidosis type IIB

Body system

Bone diseases

Inheritance pattern

X-linked recessive

Typical age of onset

Childhood

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:217093 is classified under "Bone diseases" in the Orphanet nomenclature.