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234962001: hypoplastische autosomaal dominante amelogenesis imperfecta met gladde vlakken (aandoening)


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
352125013 Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
623350018 Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6327361000146112 hypoplastische autosomaal dominante amelogenesis imperfecta met gladde vlakken nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6327371000146118 hypoplastische autosomaal dominante amelogenesis imperfecta met gladde vlakken (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6327381000146116 hypoplastische AI type ID nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Amelogenesis imperfecta, hypoplastic type true Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology congenitale hypoplasie (afwijkende morfologie) false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Jaw region structure false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure false Inferred relationship Some 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Structure of hard tissue of tooth false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Structure of hard tissue of tooth false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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