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234969005: Dentinogenesis imperfecta - Shield's type II (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
352134015 Hereditary opalescent dentine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
352135019 Dentinogenesis imperfecta without osteogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
352136018 Dentinogenesis imperfecta - Shield's type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
623358013 Dentinogenesis imperfecta - Shield's type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3890976013 Capdepont teeth en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1831581000052115 dentinogenesis imperfecta , typ 2 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dentinogenesis imperfecta - Shield's type II Is a Dentinogenesis imperfecta false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Is a Dentinogenesis imperfecta true Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Associated morphology utvecklingsabnormitet false Inferred relationship Some 3
Dentinogenesis imperfecta - Shield's type II Finding site Digestive organ structure false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Finding site Tooth structure false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Finding site Tongue structure false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Associated morphology medfödd missbildning false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Associated morphology kongenital anomali false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Occurrence Congenital false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Finding site Jaw region structure false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Finding site Oral cavity structure false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Finding site Face structure false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Finding site Digestive organ structure false Inferred relationship Some 3
Dentinogenesis imperfecta - Shield's type II Finding site Upper aerodigestive tract structure false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Finding site Tooth structure false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Associated morphology kongenital anomali false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Occurrence Congenital false Inferred relationship Some 2
Dentinogenesis imperfecta - Shield's type II Associated morphology utvecklingsabnormitet false Inferred relationship Some 2
Dentinogenesis imperfecta - Shield's type II Finding site Tooth structure false Inferred relationship Some 2
Dentinogenesis imperfecta - Shield's type II Occurrence Congenital true Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Finding site Dentin structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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