Hereditary antithrombin III deficiency 439699000
SNOMED CT code
| SNOMED code | 439699000 |
|---|---|
| name | Hereditary antithrombin III deficiency |
| status | active |
| date introduced | 2009-01-31 |
| fully specified name(s) | Hereditary antithrombin III deficiency (disorder) |
| synonyms | Hereditary antithrombin III deficiency |
| attributes - group1 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| attributes - group2 | |
| Interprets | Plasma antithrombin III activity 401039000 |
| Has interpretation | Abnormally low 371880002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Hereditary antithrombin III deficiency 439699000 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Thrombophilia 234467004 Antithrombin III deficiency 36351005 Hereditary antithrombin III deficiency 439699000 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Thrombophilia 234467004 Hereditary thrombophilia 439698008 Hereditary antithrombin III deficiency 439699000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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