Combined oxidative phosphorylation defect type 11 783558004
SNOMED CT code
| SNOMED code | 783558004 |
|---|---|
| name | Combined oxidative phosphorylation defect type 11 |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Combined oxidative phosphorylation defect type 11 (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Nervous system structure 25087005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Combined oxidative phosphorylation defect type 11 783558004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Combined oxidative phosphorylation defect type 11 783558004 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 11 783558004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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