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196286005: Dentinogenesis imperfecta (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
301910015 Dentinogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
580498015 Dentinogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4551866016 Hereditary opalescent dentin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
301910015 Dentinogenesis imperfecta en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
301910015 Dentinogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
580498015 Dentinogenesis imperfecta (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
580498015 Dentinogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4551866016 Hereditary opalescent dentin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3444251001000116 Dentinogenesis imperfecta de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
900261000172110 DGI - dentinogenèse imparfaite fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
989781000172116 dentinogenèse imparfaite fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
900261000172110 DGI - dentinogenèse imparfaite fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
989781000172116 dentinogenèse imparfaite fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3444251001000116 Dentinogenesis imperfecta de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Dentinogenesis imperfecta Is a Hereditary or idiopathic disturbance of tooth structure false Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dentinogenesis imperfecta Finding site Tongue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Finding site Oral cavity structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dentinogenesis imperfecta Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Finding site Upper aerodigestive tract structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Is a Congenital anomaly of tooth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dentinogenesis imperfecta Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dentinogenesis imperfecta Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Is a Disorder of hard tissues of teeth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta Finding site Dentin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dentinogenesis imperfecta Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Dentinogenesis imperfecta - Shield's type I Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta - Shield's type II Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta - Shield's type III Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder) Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder) Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Shell teeth Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)
Osteogenesis imperfecta, type IV B Is a True Dentinogenesis imperfecta Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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