Hereditary hypoplasminogenemia 95841006
SNOMED CT code
| SNOMED code | 95841006 |
|---|---|
| name | Hereditary hypoplasminogenemia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary hypoplasminogenemia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| parents | |
| children | Autosomal dominant deficiency of plasminogen 95842004 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary hypoplasminogenemia 95841006 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Disorder involving the fibrinolytic system 95839005 Fibrinolytic bleeding syndrome 234464006 Hypoplasminogenemia 95840007 Hereditary hypoplasminogenemia 95841006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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