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784348007: Familial congenital mirror movements (disorder)


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
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
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial congenital mirror movements survenue (attribut) congénital true Inferred relationship Some 1
Familial congenital mirror movements est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
Familial congenital mirror movements localisation d'une constatation (attribut) système nerveux true Inferred relationship Some 1
Familial congenital mirror movements est un(e) (attribut) Congenital disease true Inferred relationship Some
Familial congenital mirror movements est un(e) (attribut) Autosomal hereditary disorder true Inferred relationship Some
Familial congenital mirror movements est un(e) (attribut) Familial disease true Inferred relationship Some
Familial congenital mirror movements est un(e) (attribut) Mirror movements true Inferred relationship Some
Familial congenital mirror movements interprète (attribut) Movement (observable entity) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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