1 / 1
|
DeCS
|
|
|
Descriptor English:
|
|
Mucopolysaccharidosis II
|
Descriptor Spanish:
|
|
Mucopolisacaridosis II
|
Descriptor Portuguese:
|
|
Mucopolissacaridose II
|
Synonyms English:
|
|
Hunter Syndrome
Hunter Syndrome Gargoylism
I2S Deficiency
Mucopolysaccharidosis 2
Mucopolysaccharidosis Type 2
Mucopolysaccharidosis Type II
Deficiency, I2S
Deficiency, Iduronate 2-Sulfatase
Deficiency, Iduronate Sulfatase
Deficiency, Sulfoiduronate Sulfatase
Hunters Syndrome
Iduronate 2 Sulfatase Deficiency
Syndrome, Hunter
Syndrome, Hunter's
Gargoylism, Hunter Syndrome
Hunter's Syndrome
Iduronate 2-Sulfatase Deficiency
Iduronate Sulfatase Deficiency
Sulfoiduronate Sulfatase Deficiency
|
Tree Number:
|
|
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
|
Definition English:
|
|
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. |
Indexing Annotation English:
|
|
DF: MPS II
|
See Related English:
|
|
Iduronate Sulfatase
Mucopolysaccharidosis I
|
History Note English:
|
|
1992; for MUCOPOLYSACCHARIDOSIS 2 and HUNTER'S SYNDROME use LIPOCHONDRODYSTROPHY 1976-1991
|
Allowable Qualifiers English:
|
|
|
Record Number:
|
|
29956
|
Unique Identifier:
|
|
D016532
|
Occurrence in VHL:
|
|
|
Similar:
|
|
DeCS CID-10 SciELO LILACS LIS
|