Acyl-CoA oxidase deficiency 238069004
SNOMED CT code
SNOMED code | 238069004 |
---|---|
name | Acyl-CoA oxidase deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Acyl-coenzyme A oxidase deficiency (disorder) |
synonyms |
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attributes - group2 | |
Occurrence | Congenital 255399007 |
attributes - group1 | |
Finding site | Nervous system structure 25087005 |
Associated morphology | Degenerative abnormality 107669003 |
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 Acyl-CoA oxidase deficiency 238069004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of peroxisomal function 238059005 Loss of single peroxisomal function 238066006 Acyl-CoA oxidase deficiency 238069004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Acyl-CoA oxidase deficiency 238069004 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 oxidase deficiency 238069004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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