Disorder of mitochondrial respiratory chain complexes   237986005

SNOMED CT code


SNOMED code237986005
nameDisorder of mitochondrial respiratory chain complexes
statusactive
date introduced2002-01-31
fully specified name(s)Disorder of mitochondrial respiratory chain complexes (disorder)
synonyms
  • Mitochondrial disorder, respiratory chain
  • Disorder of mitochondrial respiratory chain complexes
attributes - group1
OccurrenceCongenital   255399007
parentsDisorder of pyruvate metabolism and mitochondrial respiratory chain   237981000
children
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome   711409002
  • Acyl-CoA dehydrogenase 9 deficiency   725046003
  • Combined oxidative phosphorylation defect type 23   1173036000
  • Combined oxidative phosphorylation defect type 26   1173034002
  • Combined oxidative phosphorylation defect type 27   1172844009
  • Combined oxidative phosphorylation defect type 29   1172843003
  • Combined oxidative phosphorylation defect type 30   1172841001
  • Deficiency in enzyme complexes of mitochondrial respiratory chain   237987001
  • Deletion and duplication of mitochondrial DNA   237994003
  • Depletion of mitochondrial DNA   237995002
  • DNA2-related mitochondrial DNA deletion syndrome   783057002
  • Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome   774205007
  • Lethal infantile mitochondrial myopathy   766251006
  • Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome   1172839002
  • Multiple mitochondrial dysfunctions syndrome   720827002
  • QRSL1-related combined oxidative phosphorylation defect   1197430005
  • Severe X-linked mitochondrial encephalomyopathy   722212004
  • Syndromic sensorineural deafness due to combined oxidative phosphorylation defect   1260133007
hierarchies
a selection of possible paths
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

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

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.