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234969005: Dentinogenesis imperfecta - Shield's type II (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
352134015 Hereditary opalescent dentine en Synonym Active Entire term case insensitive SNOMED CT core module
352135019 Dentinogenesis imperfecta without osteogenesis imperfecta en Synonym Active Entire term case insensitive SNOMED CT core module
352136018 Dentinogenesis imperfecta - Shield's type II en Synonym Active Only initial character case insensitive SNOMED CT core module
623358013 Dentinogenesis imperfecta - Shield's type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3890976013 Capdepont teeth en Synonym Active Entire term case sensitive SNOMED CT core module


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 Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Is a Dentinogenesis imperfecta true Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Dentinogenesis imperfecta - Shield's type II Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Finding site Tooth structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Finding site Tongue structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Occurrence Congenital false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Finding site Jaw region structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Finding site Oral cavity structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Finding site Face structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 3
Dentinogenesis imperfecta - Shield's type II Finding site Upper aerodigestive tract structure false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Finding site Tooth structure false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Dentinogenesis imperfecta - Shield's type II Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Dentinogenesis imperfecta - Shield's type II Finding site Tooth structure false Inferred relationship Existential restriction modifier 2
Dentinogenesis imperfecta - Shield's type II Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta - Shield's type II Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Finding site Dentin structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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