Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

SNOMED CT code


SNOMED code763721006
nameHypermethioninemia encephalopathy due to deficiency of adenosine kinase
statusactive
date introduced2018-07-31
fully specified name(s)Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder)
synonyms
  • Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
  • Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase
  • Hypermethioninemia encephalopathy due to ADK (adenosine kinase) deficiency
  • Hypermethioninaemia encephalopathy due to ADK (adenosine kinase) deficiency
attributes - group2
Due toDeficiency of adenosine kinase   124314009
attributes - group1
OccurrenceCongenital   255399007
Finding siteBrain structure   12738006
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of amino acid metabolism   44779003
            Disorder of amino acid and organic acid metabolism   237911005
              Disorder of sulfur-bearing amino acid metabolism   28882002
                Hypermethioninemia   43123004
                  Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic encephalopathy   50122000
          Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Central nervous system complication   87536007
          Hypermethioninemia encephalopathy due to deficiency of adenosine kinase   763721006

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