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234963006: Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (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
352126014 Amelogenesis imperfecta - hypoplastic autosomal dominant - rough en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
623351019 Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1852231000052114 amelogenesis imperfecta, hypoplastisk, autosomalt dominant, skrovlig yta 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
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Is a Amelogenesis imperfecta, hypoplastic type true Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Finding site Enamel structure false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Finding site Jaw region structure false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Associated morphology kongenital hypoplasi false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Occurrence Congenital false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Associated morphology Hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Associated morphology kongenital anomali false Inferred relationship Some 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Finding site Enamel structure false Inferred relationship Some 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Finding site Enamel structure true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Occurrence Congenital false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Associated morphology utvecklingsabnormitet false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Finding site Structure of hard tissue of tooth false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Finding site Structure of hard tissue of tooth false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough 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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