Hunter's syndrome
[lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase; this disease differs from muchopolysaccharidosis I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. ( CSP )]
UMLS (CSP) C0026705- Disease or Syndrome
Relation/PAR: Mucopolysaccharidoses
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