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234969005: Dentinogenesis imperfecta - Shield's type II (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
352134015 Hereditary opalescent dentine en Synonym Active Case insensitive SNOMED CT core
352135019 Dentinogenesis imperfecta without osteogenesis imperfecta en Synonym Active Case insensitive SNOMED CT core
352136018 Dentinogenesis imperfecta - Shield's type II en Synonym Active Initial character case insensitive SNOMED CT core
3890976013 Capdepont teeth en Synonym Active Case sensitive SNOMED CT core
623358013 Dentinogenesis imperfecta - Shield's type II (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dentinogenesis imperfecta - Shield's type II Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Pathological process 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 false Inferred relationship Some
Dentinogenesis imperfecta - Shield's type II Finding site Dentin structure true Inferred relationship Some 1
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 Congenital anomaly false Inferred relationship Some 1
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 Occurrence Congenital false Inferred relationship Some 2
Dentinogenesis imperfecta - Shield's type II Associated morphology Developmental abnormality 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 Associated morphology Developmental abnormality 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 Congenital malformation false Inferred relationship Some 1
Dentinogenesis imperfecta - Shield's type II Associated morphology Congenital anomaly 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 Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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