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784348007: Familial congenital mirror movements (disorder)

  • SNOMED CT Concept\Clinical finding (finding)\...
    • \Finding of movement\Movement disorder\Mirror movements\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Fetal and/or neonatal disorder\Congenital disease\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Disorder of body system\Disorder of nervous system (disorder)\Mirror movements\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Familial disease\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.
    • \Disease\Movement disorder\Mirror movements\A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5408682019 A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408683012 A rare, genetic, movement disorder characterised by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763721016 Familial congenital controlateral synkinesia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763722011 Hereditary congenital mirror movements en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763723018 Isolated congenital mirror movements en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763724012 Familial congenital mirror movements en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763725013 Hereditary congenital controlateral synkinesia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763726014 Isolated congenital controlateral synkinesia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763727017 Familial congenital mirror movements (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6228621000241119 mouvements en miroir congénitaux héréditaires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6228631000241117 syncinésie controlatérale congénitale familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6228641000241110 mouvements en miroir congénitaux familiaux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3452631001000119 Spiegelbewegungen, familiäre kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Occurrence Congenital true Inferred relationship Some 1
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Is a Hereditary disorder of nervous system true Inferred relationship Some
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Finding site Structure of nervous system (body structure) true Inferred relationship Some 1
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Is a Congenital disease true Inferred relationship Some
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Is a Autosomal hereditary disorder true Inferred relationship Some
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Is a Familial disease true Inferred relationship Some
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Is a Mirror movements true Inferred relationship Some
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Interprets mouvement false Inferred relationship Some 2
A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. Interprets Movement observable true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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