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234962001: Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth (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
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
352125013 Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5932101000241115 amélogenèse imparfaite autosomique dominante de type hypoplasique et aspect lisse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5932101000241115 amélogenèse imparfaite autosomique dominante de type hypoplasique et aspect lisse 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 - smooth Is a Amelogenesis imperfecta, hypoplastic type true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth 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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