784348007: Familial congenital mirror movements (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of movement\Movement disorder\Mirror movements\A rare genetic movement disorder with characteristics of 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 with characteristics of 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 with characteristics of 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 foetus and/or newborn\Congenital disease\A rare genetic movement disorder with characteristics of 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 with characteristics of 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 with characteristics of 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 with characteristics of 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 (disorder)\A rare genetic movement disorder with characteristics of 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 with characteristics of 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

3763728010 A rare genetic movement disorder with characteristics of 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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A rare genetic movement disorder with characteristics of 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 with characteristics of 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 with characteristics of 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 with characteristics of 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 with characteristics of 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 with characteristics of 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 (disorder)	true	Inferred relationship	Some
A rare genetic movement disorder with characteristics of 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 with characteristics of 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	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3763728010	A rare genetic movement disorder with characteristics of 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