Combined oxidative phosphorylation defect type 17 775908005
SNOMED CT code
SNOMED code | 775908005 |
---|---|
name | Combined oxidative phosphorylation defect type 17 |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Combined oxidative phosphorylation defect type 17 (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Myocardium structure 74281007 |
Associated morphology | Hypertrophy 56246009 |
attributes - group2 | |
Due to | Mitochondrial cytopathy 240096000 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical 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 | sorted most to least specific
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cpt crosswalks |
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