SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Enzymopathy  78548001

Citrullinemia  398680004

Citrin deficiency   429735007

SNOMED CT code


SNOMED code429735007
nameCitrin deficiency
statusactive
date introduced2008-01-31
fully specified name(s)Citrin deficiency (disorder)
synonyms
  • Citrin deficiency
  • SLC25A13 related citrin deficiency
  • Solute carrier family 25 member 13 related citrin deficiency
parents
childrenCitrullinemia type II   716863007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Enzymopathy   78548001
          Citrullinemia   398680004
            Citrin deficiency   429735007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Citrin deficiency   429735007

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

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