Homozygous methylenetetrahydrofolate reductase mutation 139811000119109
SNOMED CT code
SNOMED code | 139811000119109 |
---|---|
name | Homozygous methylenetetrahydrofolate reductase mutation |
status | active |
date introduced | 2015-01-31 |
fully specified name(s) | Homozygous methylenetetrahydrofolate reductase mutation (disorder) |
synonyms | Homozygous 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 Homozygous methylenetetrahydrofolate reductase mutation 139811000119109 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Homozygous methylenetetrahydrofolate reductase mutation 139811000119109 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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