Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency   721236002

SNOMED CT code


SNOMED code721236002
nameHyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
statusactive
date introduced2017-01-31
fully specified name(s)Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)
synonyms
  • Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
  • Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
attributes - group2
Due toShort chain 3-hydroxyacyl-CoA dehydrogenase deficiency   237998000
attributes - group1
OccurrenceCongenital   255399007
Finding siteEndocrine pancreatic structure   78696007
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency   721236002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency   721236002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency   721236002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of carbohydrate metabolism   20957000
          Disorder of glucose regulation   237597000
            Hyperinsulinism   83469008
              Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency   721236002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency   721236002

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