Combined oxidative phosphorylation defect type 29   1172843003

SNOMED CT code


SNOMED code1172843003
nameCombined oxidative phosphorylation defect type 29
statusactive
date introduced2021-09-30
fully specified name(s)Combined oxidative phosphorylation defect type 29 (disorder)
synonyms
  • Combined oxidative phosphorylation defect type 29
  • COXPD29 - combined oxidative phosphorylation defect type 29
attributes - group2
OccurrenceCongenital   255399007
attributes - group1
Finding siteCerebellar structure   113305005
Associated morphologyAtrophy   13331008
parents
  • Inherited metabolic disorder of nervous system   128190004
  • Disorder of mitochondrial respiratory chain complexes   237986005
  • Mitochondrial cytopathy   240096000
  • Hereditary cerebellar atrophy   431641000124107
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Inherited metabolic disorder of nervous system   128190004
            Combined oxidative phosphorylation defect type 29   1172843003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Disorder of pyruvate metabolism and mitochondrial respiratory chain   237981000
            Disorder of mitochondrial respiratory chain complexes   237986005
              Combined oxidative phosphorylation defect type 29   1172843003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Mitochondrial cytopathy   240096000
          Combined oxidative phosphorylation defect type 29   1172843003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Hereditary degenerative disease of central nervous system   106018006
            Hereditary cerebellar degeneration   37650008
              Hereditary cerebellar atrophy   431641000124107
                Combined oxidative phosphorylation defect type 29   1172843003

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 29   1172843003

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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