FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

234965004: Amelogenesis imperfecta - hypomaturation - recessive pigmented (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
352128010 Amelogenesis imperfecta - hypomaturation - recessive pigmented en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
623354010 Amelogenesis imperfecta - hypomaturation - recessive pigmented (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
352128010 Amelogenesis imperfecta - hypomaturation - recessive pigmented en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
352128010 Amelogenesis imperfecta - hypomaturation - recessive pigmented en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
623354010 Amelogenesis imperfecta - hypomaturation - recessive pigmented (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
623354010 Amelogenesis imperfecta - hypomaturation - recessive pigmented (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5982091000241115 amélogenèse imparfaite récessive de type hypomature pigmenté fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5982091000241115 amélogenèse imparfaite récessive de type hypomature pigmenté 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 - hypomaturation - recessive pigmented Is a Amelogenesis imperfecta, hypomaturation type (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypomaturation - recessive pigmented Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypomaturation - recessive pigmented Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta - hypomaturation - recessive pigmented Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta - hypomaturation - recessive pigmented Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta - hypomaturation - recessive pigmented Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypomaturation - recessive pigmented Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypomaturation - recessive pigmented Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta - hypomaturation - recessive pigmented Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta - hypomaturation - recessive pigmented Pathological process (attribute) Pathological developmental process (qualifier value) 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

Back to Start