Hereditary factor XIII deficiency disease 50189006
SNOMED CT code
| SNOMED code | 50189006 |
|---|---|
| name | Hereditary factor XIII deficiency disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary factor XIII deficiency disease (disorder) |
| synonyms |
|
| 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 factor XIII deficiency disease 50189006 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Coagulation factor deficiency syndrome 86075001 Factor XIII deficiency disease 18604004 Hereditary factor XIII deficiency disease 50189006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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