Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002
SNOMED CT code
| SNOMED code | 764962002 |
|---|---|
| name | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) |
| synonyms |
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| attributes - group3 | |
| Due to | Disease of liver 235856003 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Brain structure 12738006 |
| attributes - group1 | |
| Finding site | Liver structure 10200004 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic encephalopathy 50122000 Hepatic encephalopathy 13920009 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic and genetic disorder affecting the liver 235903001 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 764962002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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