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699328003: Myoclonic epilepsy myopathy sensory ataxia (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myoclonic epilepsy myopathy sensory ataxia Is a Spinocerebellar disease true Inferred relationship Existential restriction modifier
Myoclonic epilepsy myopathy sensory ataxia Is a Depletion of mitochondrial deoxyribonucleic acid true Inferred relationship Existential restriction modifier
Myoclonic epilepsy myopathy sensory ataxia Is a Hereditary cerebellar degeneration true Inferred relationship Existential restriction modifier
Myoclonic epilepsy myopathy sensory ataxia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Myoclonic epilepsy myopathy sensory ataxia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Myoclonic epilepsy myopathy sensory ataxia Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Myoclonic epilepsy myopathy sensory ataxia Associated morphology Degeneration false Inferred relationship Existential restriction modifier 4
Myoclonic epilepsy myopathy sensory ataxia Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 3
Myoclonic epilepsy myopathy sensory ataxia Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 4
Myoclonic epilepsy myopathy sensory ataxia Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Myoclonic epilepsy myopathy sensory ataxia Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Myoclonic epilepsy myopathy sensory ataxia Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 3
Myoclonic epilepsy myopathy sensory ataxia Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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