Defect of purinergic receptor p2y G protein-coupled 12 725291001
SNOMED CT code
| SNOMED code | 725291001 |
|---|---|
| name | Defect of purinergic receptor p2y G protein-coupled 12 |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Defect of purinergic receptor p2y G protein-coupled 12 (disorder) |
| synonyms |
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| attributes - group2 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of hematological system 414387006 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Platelet disorder 22716005 Inherited platelet disorder 234469001 Hereditary platelet function disorder 128096008 Defect of purinergic receptor p2y G protein-coupled 12 725291001 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Blood coagulation disorder 64779008 Defect of purinergic receptor p2y G protein-coupled 12 725291001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Defect of purinergic receptor p2y G protein-coupled 12 725291001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Defect of purinergic receptor p2y G protein-coupled 12 725291001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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