SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Disorder of lysosomal enzyme  23585005

Mucopolysaccharidosis  11380006

Mucopolysaccharidosis, MPS-II   70737009

SNOMED CT code


SNOMED code70737009
nameMucopolysaccharidosis, MPS-II
statusactive
date introduced2002-01-31
fully specified name(s)Mucopolysaccharidosis type II (disorder)
synonyms
  • Mucopolysaccharidosis, MPS-II
  • Hunter's syndrome
  • Sulfoiduronidate sulfatase deficiency
  • Iduronate 2-sulfatase deficiency
  • Hunter syndrome
  • Hunter disease
  • MPSII - Mucopolysaccharidosis type II
  • Mucopolysaccharidosis type II
  • MPS 2 - Mucopolysaccharidosis 2
  • Deficiency of iduronate-2-sulfatase
  • Iduronate 2-sulphatase deficiency
  • Sulphoiduronidate sulphatase deficiency
  • Iduronate sulphatase deficiency
  • Sulpho-iduronate sulphatase deficiency
  • Iduronate sulfatase deficiency
  • Sulfo-iduronate sulfatase deficiency
  • Deficiency of iduronate-2-sulphatase
attributes - group1
OccurrenceCongenital   255399007
attributes - group2
Finding siteLiver structure   10200004
parents
  • Mucopolysaccharidosis   11380006
  • X-linked recessive hereditary disease   1162976004
  • Metabolic and genetic disorder affecting the liver   235903001
  • Digestive system hereditary disorder   363080007
children
  • Hunter's syndrome, mild form   5667009
  • Hunter's syndrome, severe form   73146005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Disorder of lysosomal enzyme   23585005
          Mucopolysaccharidosis   11380006
            Mucopolysaccharidosis, MPS-II   70737009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked recessive hereditary disease   1162976004
                Mucopolysaccharidosis, MPS-II   70737009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic and genetic disorder affecting the liver   235903001
          Mucopolysaccharidosis, MPS-II   70737009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Mucopolysaccharidosis, MPS-II   70737009

ancestors
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