Hereditary factor XIII B subunit deficiency 439459008
SNOMED CT code
SNOMED code | 439459008 |
---|---|
name | Hereditary factor XIII B subunit deficiency |
status | active |
date introduced | 2009-01-31 |
fully specified name(s) | Hereditary factor XIII B subunit deficiency (disorder) |
synonyms |
|
attributes - group1 | |
Interprets | Hemostatic function 74848003 |
Has interpretation | Abnormal 263654008 |
parents | Hereditary factor XIII deficiency disease 50189006 |
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 Hereditary factor XIII deficiency disease 50189006 Hereditary factor XIII B subunit deficiency 439459008 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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