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196286005: Dentinogenesis imperfecta (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
301910015 Dentinogenesis imperfecta en Synonym Active Entire term case insensitive SNOMED CT core module
580498015 Dentinogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4551866016 Hereditary opalescent dentin en Synonym Active Entire term case insensitive SNOMED CT core module

9 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dentinogenesis imperfecta Is a Congenital anomaly of teeth false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Is a Hereditary or idiopathic disturbance of tooth structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 3
Dentinogenesis imperfecta Finding site Tongue structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Finding site Jaw region structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Occurrence Congenital false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Finding site Oral cavity structure false Inferred relationship Existential restriction modifier 3
Dentinogenesis imperfecta Finding site Face structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Finding site Upper aerodigestive tract structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Is a Congenital anomaly of tooth true Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Dentinogenesis imperfecta Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier 2
Dentinogenesis imperfecta Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Is a Disorder of hard tissues of teeth true Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta Finding site Dentin structure true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Dentinogenesis imperfecta - Shield's type I Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type III Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Shell teeth Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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