Hereditary factor XI deficiency disease 49762007
SNOMED CT code
| SNOMED code | 49762007 |
|---|---|
| name | Hereditary factor XI deficiency disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary factor XI deficiency disease (disorder) |
| synonyms |
|
| attributes - group2 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Hemostatic function 74848003 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Contact factor deficiency 234452003 Hereditary factor XI deficiency disease 49762007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary factor XI deficiency disease 49762007 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 XI deficiency 767713001 Hereditary factor XI deficiency disease 49762007 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 XI deficiency disease 49762007 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Coagulation factor deficiency syndrome 86075001 Hemophilia 90935002 Hereditary factor XI deficiency disease 49762007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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