Dentinogenesis imperfecta - Shield's type I 234968002
SNOMED CT code
SNOMED code | 234968002 |
---|---|
name | Dentinogenesis imperfecta - Shield's type I |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Dentinogenesis imperfecta - Shield's type I (disorder) |
synonyms |
|
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Dentin structure 84540008 |
Occurrence | Congenital 255399007 |
parents | Dentinogenesis imperfecta 196286005 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Dentinogenesis imperfecta 196286005 Dentinogenesis imperfecta - Shield's type I 234968002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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