Congenital plasminogen activator inhibitor deficiency type 1 717407006
SNOMED CT code
SNOMED code | 717407006 |
---|---|
name | Congenital plasminogen activator inhibitor deficiency type 1 |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Congenital plasminogen activator inhibitor deficiency type 1 (disorder) |
synonyms | Congenital plasminogen activator inhibitor deficiency type 1 |
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 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary coagulation factor deficiency 16922007 Congenital plasminogen activator inhibitor deficiency type 1 717407006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital plasminogen activator inhibitor deficiency type 1 717407006 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 plasminogen activator inhibitor deficiency type 1 717407006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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