Hereditary factor X deficiency disease 37350004
SNOMED CT code
| SNOMED code | 37350004 |
|---|---|
| name | Hereditary factor X deficiency disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary factor X deficiency disease (disorder) |
| synonyms |
|
| 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 Hereditary coagulation factor deficiency 16922007 Hereditary factor X deficiency disease 37350004 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Prothrombin complex deficiency 234454002 Factor X deficiency 76642003 Hereditary factor X deficiency disease 37350004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hereditary factor X deficiency disease 37350004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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