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276701009: Fetal cytomegalovirus syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
299711000077115 embryopathie à cytomégalovirus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3010599018 Foetal cytomegalovirus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412971017 Fetal cytomegalovirus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
582291000077115 embryopathie à cytomégalovirus (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
669648013 Fetal cytomegalovirus syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
910941000172118 infection anténatale au CMV fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
embryopathie à cytomégalovirus Causative agent Genus Cytomegalovirus (organism) true Inferred relationship Some 1
embryopathie à cytomégalovirus survenue (attribut) période fœtale true Inferred relationship Some 1
embryopathie à cytomégalovirus est un(e) (attribut) Infectious disorder of the fetus false Inferred relationship Some
embryopathie à cytomégalovirus est un(e) (attribut) infection virale selon la localisation false Inferred relationship Some
embryopathie à cytomégalovirus est un(e) (attribut) infection à cytomégalovirus true Inferred relationship Some
embryopathie à cytomégalovirus localisation d'une constatation (attribut) Fetal structure false Inferred relationship Some
embryopathie à cytomégalovirus survenue (attribut) période fœtale false Inferred relationship Some
embryopathie à cytomégalovirus Causative agent Cytomegalovirus group virus false Inferred relationship Some
embryopathie à cytomégalovirus Causative agent Genus Cytomegalovirus (organism) false Inferred relationship Some
embryopathie à cytomégalovirus survenue (attribut) période fœtale false Inferred relationship Some
embryopathie à cytomégalovirus Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some
embryopathie à cytomégalovirus processus pathologique maladie infectieuse false Inferred relationship Some
embryopathie à cytomégalovirus survenue (attribut) Perinatal state (finding) false Inferred relationship Some
embryopathie à cytomégalovirus survenue (attribut) congénital false Inferred relationship Some
embryopathie à cytomégalovirus Causative agent Human cytomegalovirus 5 (organism) false Inferred relationship Some
embryopathie à cytomégalovirus Causative agent Betaherpesvirus group false Inferred relationship Some
embryopathie à cytomégalovirus est un(e) (attribut) Infectious disorder of the fetus true Inferred relationship Some
embryopathie à cytomégalovirus est un(e) (attribut) Fetal disorder false Inferred relationship Some
embryopathie à cytomégalovirus Pathological process (attribute) Infectious process (qualifier value) true Inferred relationship Some 1
embryopathie à cytomégalovirus Causative agent Familia Herpesviridae false Inferred relationship Some 1
embryopathie à cytomégalovirus Causative agent Subfamily Betaherpesvirinae (organism) false Inferred relationship Some 2
embryopathie à cytomégalovirus Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some 2
embryopathie à cytomégalovirus est un(e) (attribut) Congenital cytomegalovirus infection (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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