Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein 720461006
SNOMED CT code
SNOMED code | 720461006 |
---|---|
name | Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder) |
synonyms | Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein |
attributes - group1 | |
Finding site | Liver structure 10200004 |
Occurrence | Infancy 3658006 |
attributes - group2 | |
Clinical course | Sudden onset AND/OR short duration 424124008 |
attributes - group3 | |
Due to | Disorder of mitochondrial respiratory chain complexes 237986005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Acute disease 2704003 Acute digestive system disorder 127321000 Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein 720461006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Hepatic failure 59927004 Acute hepatic failure 197270009 Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein 720461006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein 720461006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein 720461006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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