FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term mucopolysaccharidosis II ID (Ontology) DOID:12799 (Human Disease)
Definition A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase.
Also Known As "deficiency of iduronate-2-sulphatase" ; "Hunter syndrome" ; "Hunter's syndrome" (for all, see Synonyms field below)
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 Genes
 mucopolysaccharidosis II       1
 for disease ribbon | mucopolysaccharidosis II       1
 model of | mucopolysaccharidosis II       1
Spanning Tree (Parents/Children)
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  lysosomal storage disease
   |__mucopolysaccharidosis
       |__mucopolysaccharidosis II  1 rec.
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Is a mucopolysaccharidosis
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Synonyms
  • "deficiency of iduronate-2-sulphatase" EXACT
    "Hunter syndrome" EXACT
    "Hunter's syndrome" EXACT
    "MPS II - Hunter syndrome" EXACT
    "Mucopolysaccharidosis, MPS-II" EXACT
Secondary IDs
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GARD:6675
ICD10CM:E76.1
MESH:D016532
MIM:309900
NCI:C61260
SNOMEDCT_US_2023_03_01:190936000
UMLS_CUI:C0026705