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234961008: Amelogenesis imperfecta - hypoplastic autosomal dominant - local (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
352124012 Amelogenesis imperfecta - hypoplastic autosomal dominant - local en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
623349018 Amelogenesis imperfecta - hypoplastic autosomal dominant - local (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1806921000052111 amelogenesis imperfecta, hypoplastisk, autosomalt dominant, lokal 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 - local Is a Amelogenesis imperfecta, hypoplastic type true Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Finding site Enamel structure true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Finding site Jaw region structure false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Associated morphology kongenital hypoplasi false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Occurrence Congenital false Inferred relationship Some
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Associated morphology Hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Associated morphology kongenital anomali false Inferred relationship Some 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Finding site Enamel structure false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Finding site Enamel structure false Inferred relationship Some 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Occurrence Congenital false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Associated morphology utvecklingsabnormitet false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Finding site Structure of hard tissue of tooth false Inferred relationship Some 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Finding site Structure of hard tissue of tooth false Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local 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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