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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
352126014 Amelogenesis imperfecta - hypoplastic autosomal dominant - rough en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5942031000241112 amélogenèse imparfaite autosomique dominante de type hypoplasique et aspect rugueux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5942031000241112 amélogenèse imparfaite autosomique dominante de type hypoplasique et aspect rugueux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Is a Amelogenesis imperfecta, hypoplastic type true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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