Heterozygous methylenetetrahydrofolate reductase mutation 139821000119102
SNOMED CT code
| SNOMED code | 139821000119102 |
|---|---|
| name | Heterozygous methylenetetrahydrofolate reductase mutation |
| status | active |
| date introduced | 2015-01-31 |
| fully specified name(s) | Heterozygous methylenetetrahydrofolate reductase mutation (disorder) |
| synonyms | Heterozygous methylenetetrahydrofolate reductase mutation |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Endocrine structure 113331007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Heterozygous methylenetetrahydrofolate reductase mutation 139821000119102 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Heterozygous methylenetetrahydrofolate reductase mutation 139821000119102 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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