Dentinogenesis imperfecta 196286005
SNOMED CT code
| SNOMED code | 196286005 |
|---|---|
| name | Dentinogenesis imperfecta |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Dentinogenesis imperfecta (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Dentin structure 84540008 |
| Occurrence | Congenital 255399007 |
| parents |
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| children |
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| 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 Dentinogenesis imperfecta 196286005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary disorder of tooth 1148766007 Dentinogenesis imperfecta 196286005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Dentinogenesis imperfecta 196286005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of mouth region 423066003 Oral cavity finding 116337000 Congenital abnormality of oral cavity 282041002 Congenital anomaly of tooth 422977003 Dentinogenesis imperfecta 196286005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Disorder of digestive organ 76712006 Tooth disorder 234947003 Disorder of hard tissues of teeth 46557008 Dentinogenesis imperfecta 196286005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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