Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 720951008
SNOMED CT code
| SNOMED code | 720951008 |
|---|---|
| name | Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder) |
| synonyms |
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| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 720951008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 720951008 |
| ancestors | sorted most to least specific |
| cpt crosswalks |
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