Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.

Descriptor ID	D016532
MeSH Number(s)	C10.597.606.643.455.750 C16.320.322.500.750 C16.320.400.525.750 C16.320.565.202.715.645 C16.320.565.595.600.645 C17.300.550.575.645 C18.452.648.202.715.645 C18.452.648.595.600.645
Concept/Terms	Mucopolysaccharidosis II Mucopolysaccharidosis II Hunter Syndrome Gargoylism Hunter's Syndrome Hunters Syndrome Syndrome, Hunter's Mucopolysaccharidosis Type 2 Mucopolysaccharidosis Type II Hunter Syndrome Syndrome, Hunter Gargoylism, Hunter Syndrome Mucopolysaccharidosis 2 Sulfoiduronate Sulfatase Deficiency Sulfoiduronate Sulfatase Deficiency Deficiency, Sulfoiduronate Sulfatase Iduronate Sulfatase Deficiency Deficiency, Iduronate Sulfatase I2S Deficiency Deficiency, I2S Iduronate 2-Sulfatase Deficiency Deficiency, Iduronate 2-Sulfatase Iduronate 2 Sulfatase Deficiency

Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidosis II".

Below are MeSH descriptors whose meaning is related to "Mucopolysaccharidosis II".

Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidosis II".