Hereditary von Willebrand disease type 2B 359717002
SNOMED CT code
| SNOMED code | 359717002 |
|---|---|
| name | Hereditary von Willebrand disease type 2B |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary von Willebrand disease type 2B (disorder) |
| synonyms | Hereditary von Willebrand disease type 2B |
| attributes - group1 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| 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 von Willebrand disease type 2B 359717002 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 von Willebrand disorder 128105004 Hereditary von Willebrand disease 1259242002 Hereditary von Willebrand disease type 2 128107007 Hereditary von Willebrand disease type 2B 359717002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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