Hereditary combined coagulation factor deficiency 439157002
SNOMED CT code
| SNOMED code | 439157002 |
|---|---|
| name | Hereditary combined coagulation factor deficiency |
| status | active |
| date introduced | 2009-01-31 |
| fully specified name(s) | Hereditary combined coagulation factor deficiency (disorder) |
| synonyms | Hereditary combined coagulation factor deficiency |
| attributes - group1 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary coagulation factor deficiency 16922007 Hereditary combined coagulation factor deficiency 439157002 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Coagulation factor deficiency syndrome 86075001 Combined coagulation factor deficiency 234463000 Hereditary combined coagulation factor deficiency 439157002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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