Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism 109472008
SNOMED CT code
SNOMED code | 109472008 |
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name | Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Enamel structure 76993005 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Abnormal shape 399984000 |
Finding site | Tooth structure 38199008 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Amelogenesis imperfecta 78494001 Amelogenesis imperfecta, hypomaturation type 109475005 Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism 109472008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Amelogenesis imperfecta 78494001 Amelogenesis imperfecta, hypoplastic type 109476006 Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism 109472008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Taurodontism 51744007 Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism 109472008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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