Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 783250007
SNOMED CT code
SNOMED code | 783250007 |
---|---|
name | Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency |
status | active |
date introduced | 2019-07-31 |
fully specified name(s) | Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder) |
synonyms | Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency |
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 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 783250007 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Thrombophilia 234467004 Hereditary thrombophilia 439698008 Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 783250007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 783250007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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