Congenital defect of folate absorption 62578003
SNOMED CT code
| SNOMED code | 62578003 |
|---|---|
| name | Congenital defect of folate absorption |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Congenital defect of folate absorption (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 organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disorder of sulfur-bearing amino acid metabolism 28882002 Congenital defect of folate absorption 62578003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Inherited disorder of folate metabolism 4702003 Congenital defect of folate absorption 62578003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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