Acyl-CoA dehydrogenase 9 deficiency 725046003
SNOMED CT code
SNOMED code | 725046003 |
---|---|
name | Acyl-CoA dehydrogenase 9 deficiency |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9 (disorder) |
synonyms |
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attributes - group2 | |
Due to | Acyl-CoA dehydrogenase deficiency 82319005 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of pyruvate metabolism and mitochondrial respiratory chain 237981000 Disorder of mitochondrial respiratory chain complexes 237986005 Acyl-CoA dehydrogenase 9 deficiency 725046003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Acyl-CoA dehydrogenase 9 deficiency 725046003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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