Combined oxidative phosphorylation defect type 17   775908005

SNOMED CT code


SNOMED code775908005
nameCombined oxidative phosphorylation defect type 17
statusactive
date introduced2019-01-31
fully specified name(s)Combined oxidative phosphorylation defect type 17 (disorder)
synonyms
  • COXPD17 - combined oxidative phosphorylation defect type 17
  • Combined oxidative phosphorylation defect type 17
attributes - group1
Finding siteMyocardium structure   74281007
Associated morphologyHypertrophy   56246009
attributes - group2
Due toMitochondrial cytopathy   240096000
parents
  • Mitochondrial cytopathy   240096000
  • Cardiovascular system hereditary disorder   363005004
  • Hypertrophic mitochondrial cardiomyopathy   472316006
  • 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
          Combined oxidative phosphorylation defect type 17   775908005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Combined oxidative phosphorylation defect type 17   775908005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Cardiac finding   301095005
        Heart disease   56265001
          Cardiac complication   40172005
            Mitochondrial cardiomyopathy   472315005
              Hypertrophic mitochondrial cardiomyopathy   472316006
                Combined oxidative phosphorylation defect type 17   775908005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Combined oxidative phosphorylation defect type 17   775908005

ancestors
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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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