Hereditary factor IX deficiency disease 41788008
SNOMED CT code
| SNOMED code | 41788008 |
|---|---|
| name | Hereditary factor IX deficiency disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary factor IX 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 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 Hereditary factor IX deficiency disease 41788008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary factor IX deficiency disease 41788008 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 IX deficiency 767712006 Hereditary factor IX deficiency disease 41788008 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 IX deficiency disease 41788008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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