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 IIs, Mucopolysaccharidosis Mucopolysaccharidosis IIs Mucopolysaccharidosis Type 2 2, Mucopolysaccharidosis Type 2s, Mucopolysaccharidosis Type Mucopolysaccharidosis Type 2s Type 2, Mucopolysaccharidosis Type 2s, Mucopolysaccharidosis Hunter's Syndrome Hunter Syndrome Hunters Syndrome Syndrome, Hunter's Mucopolysaccharidosis 2 Gargoylism, Hunter Syndrome Hunter Syndrome Gargoylism Sulfoiduronate Sulfatase Deficiency Sulfoiduronate Sulfatase Deficiency Deficiencies, Sulfoiduronate Sulfatase Deficiency, Sulfoiduronate Sulfatase Sulfatase Deficiencies, Sulfoiduronate Sulfatase Deficiency, Sulfoiduronate Sulfoiduronate Sulfatase Deficiencies Iduronate Sulfatase Deficiency Deficiencies, Iduronate Sulfatase Deficiency, Iduronate Sulfatase Iduronate Sulfatase Deficiencies Sulfatase Deficiencies, Iduronate Sulfatase Deficiency, Iduronate Iduronate 2-Sulfatase Deficiency Deficiencies, Iduronate 2-Sulfatase Deficiency, Iduronate 2-Sulfatase Iduronate 2 Sulfatase Deficiency Iduronate 2-Sulfatase Deficiencies

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".