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733065003: Myoclonus, cerebellar ataxia, deafness syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3498660011 Myoclonus, cerebellar ataxia, deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3498661010 Myoclonus, cerebellar ataxia, deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403703018 This syndrome is characterized by the association of myoclonus, cerebellar ataxia and sensorineural hearing loss. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403704012 This syndrome is characterised by the association of myoclonus, cerebellar ataxia and sensorineural hearing loss. 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
Myoclonus, cerebellar ataxia, deafness syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Sensorineural hearing loss false Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Extrapyramidal disease true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Cerebellar ataxia true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Congenital hearing disorder false Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Myoclonic disorder true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Hearing loss associated with syndrome true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Hereditary disorder of nervous system false Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Interprets Hearing true Inferred relationship Some 3
Myoclonus, cerebellar ataxia, deafness syndrome Interprets Functional observable false Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Occurrence Congenital true Inferred relationship Some 4
Myoclonus, cerebellar ataxia, deafness syndrome Finding site Cerebellar structure true Inferred relationship Some 4
Myoclonus, cerebellar ataxia, deafness syndrome Occurrence Congenital true Inferred relationship Some 5
Myoclonus, cerebellar ataxia, deafness syndrome Finding site Ear structure true Inferred relationship Some 5
Myoclonus, cerebellar ataxia, deafness syndrome Is a Hereditary ataxia (disorder) true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Congenital sensorineural hearing loss (disorder) true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a Disorder of ear true Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Interprets Movement true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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