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DeCS
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Descriptor English:
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Mucopolysaccharidosis II
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Descriptor Spanish:
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mucopolisacaridosis II
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Descriptor Portuguese:
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Mucopolissacaridose II
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Synonyms English:
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Deficiency, I2S
Deficiency, Iduronate 2-Sulfatase
Deficiency, Iduronate Sulfatase
Deficiency, Sulfoiduronate Sulfatase
Gargoylism, Hunter Syndrome
Hunter Syndrome
Hunter Syndrome Gargoylism
Hunter's Syndrome
Hunters Syndrome
I2S Deficiency
Iduronate 2 Sulfatase Deficiency
Iduronate 2-Sulfatase Deficiency
Iduronate Sulfatase Deficiency
Mucopolysaccharidosis 2
Mucopolysaccharidosis Type 2
Mucopolysaccharidosis Type II
Sulfoiduronate Sulfatase Deficiency
Syndrome, Hunter
Syndrome, Hunter's
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Tree Number:
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C10.597.606.360.455.750
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
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Definition English:
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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. |
See Related English:
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Iduronate Sulfatase
Mucopolysaccharidosis I
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History Note English:
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1992; for MUCOPOLYSACCHARIDOSIS 2 and HUNTER'S SYNDROME use LIPOCHONDRODYSTROPHY 1976-1991
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Allowable Qualifiers English:
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Record Number:
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29956
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Unique Identifier:
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D016532
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Occurrence in VHL:
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Similar:
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DeCS
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