Hereditary congenital prekallikrein deficiency 1162804003
SNOMED CT code
| SNOMED code | 1162804003 |
|---|---|
| name | Hereditary congenital prekallikrein deficiency |
| status | active |
| date introduced | 2021-09-30 |
| fully specified name(s) | Hereditary congenital prekallikrein deficiency (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| parents | |
| 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 Prekallikrein deficiency 48976006 Hereditary congenital prekallikrein deficiency 1162804003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary congenital prekallikrein deficiency 1162804003 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 congenital prekallikrein deficiency 1162804003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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