SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Mitochondrial cytopathy  240096000

Combined oxidative phosphorylation defect type 28   1187640000

SNOMED CT code


SNOMED code1187640000
nameCombined oxidative phosphorylation defect type 28
statusactive
date introduced2022-01-31
fully specified name(s)Combined oxidative phosphorylation defect type 28 (disorder)
synonyms
  • COXPD28 - combined oxidative phosphorylation defect type 28
  • Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
  • Combined oxidative phosphorylation defect type 28
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
          Combined oxidative phosphorylation defect type 28   1187640000

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 28   1187640000

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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