Autosomal dominant hereditary disorder
Congenital anomaly of tooth
Developmental hereditary disorder
Disorder of hard tissues of teeth
Hereditary disorder of tooth
|||||
Dentinogenesis imperfecta (disorder)
Dentinogenesis imperfecta
Hereditary opalescent dentin
dentinogenesis imperfecta
DGI
Id196286005
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteDentin structure
OccurrenceCongenital
Pathological processPathological developmental process
PALGA thesaurus simple reference set for pathology
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetK00.5
RuleTRUE
AdviceALWAYS K00.5
CorrelationSNOMED CT source code to target map code correlation not specified
|
Dentinogenesis imperfecta - Shield's type I
Dentinogenesis imperfecta - Shield's type II
Dentinogenesis imperfecta - Shield's type III
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
Goldblatt syndrome
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta
Osteogenesis imperfecta, type IV B
Shell teeth
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome