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699328003: Myoclonic epilepsy myopathy sensory ataxia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2983908011 MEMSA - myoclonic epilepsy myopathy sensory ataxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983919014 Spinocerebellar ataxia with epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983928010 Myoclonic epilepsy myopathy sensory ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983952015 Myoclonic epilepsy myopathy sensory ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myoclonic epilepsy myopathy sensory ataxia (disorder) localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 1
Myoclonic epilepsy myopathy sensory ataxia (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Myoclonic epilepsy myopathy sensory ataxia (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 3
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) Inherited metabolic disorder of nervous system true Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) Spinocerebellar disease true Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) Depletion of mitochondrial deoxyribonucleic acid (disorder) true Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) Hereditary cerebellar degeneration true Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Myoclonic epilepsy myopathy sensory ataxia (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 3
Myoclonic epilepsy myopathy sensory ataxia (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 4
Myoclonic epilepsy myopathy sensory ataxia (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 3
Myoclonic epilepsy myopathy sensory ataxia (disorder) localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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