SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Mitochondrial cytopathy  240096000

Childhood myocerebrohepatopathy spectrum   702366001

SNOMED CT code


SNOMED code702366001
nameChildhood myocerebrohepatopathy spectrum
statusactive
date introduced2014-07-31
fully specified name(s)Childhood myocerebrohepatopathy spectrum (disorder)
synonymsChildhood myocerebrohepatopathy spectrum
attributes - group1
OccurrenceChildhood   255398004
parents
  • Mitochondrial cytopathy   240096000
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Mitochondrial cytopathy   240096000
          Childhood myocerebrohepatopathy spectrum   702366001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Childhood myocerebrohepatopathy spectrum   702366001

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.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

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