Aminomethyltransferase deficiency 67845009
SNOMED CT code
| SNOMED code | 67845009 |
|---|---|
| name | Aminomethyltransferase deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Aminomethyltransferase deficiency (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of acid-base balance 26436007 Acidemia 70731005 Aminoacidemia 46556004 Hyperglycinemia 64654004 Non-ketotic hyperglycinemia 237939006 Aminomethyltransferase deficiency 67845009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Aminomethyltransferase deficiency 67845009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Aminomethyltransferase deficiency 67845009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Aminomethyltransferase deficiency 67845009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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