Congenital alpha-2-antiplasmin deficiency 716746003
SNOMED CT code
| SNOMED code | 716746003 |
|---|---|
| name | Congenital alpha-2-antiplasmin deficiency |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Congenital alpha-2-antiplasmin deficiency (disorder) |
| synonyms |
|
| attributes - group2 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Hemostatic function 74848003 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| 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 Disorder involving the fibrinolytic system 95839005 Fibrinolytic bleeding syndrome 234464006 Alpha-2-antiplasmin deficiency 234465007 Congenital alpha-2-antiplasmin deficiency 716746003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital alpha-2-antiplasmin deficiency 716746003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital alpha-2-antiplasmin deficiency 716746003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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