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


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

Descriptions:

Id Description Lang Type Status Case? Module
3498660011 Myoclonus, cerebellar ataxia, deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3498661010 Myoclonus, cerebellar ataxia, deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


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 Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Sensorineural hearing loss false Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Extrapyramidal disease true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Myoclonic disorder true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Myoclonus, cerebellar ataxia, deafness syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Myoclonus, cerebellar ataxia, deafness syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 4
Myoclonus, cerebellar ataxia, deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Myoclonus, cerebellar ataxia, deafness syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 5
Myoclonus, cerebellar ataxia, deafness syndrome Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Is a Disorder of ear true Inferred relationship Existential restriction modifier
Myoclonus, cerebellar ataxia, deafness syndrome Interprets Movement true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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