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699328003: Myoclonic epilepsy myopathy sensory ataxia (disorder)


Status: current, Primitive. 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 Active Initial character case insensitive SNOMED CT core
2983919014 Spinocerebellar ataxia with epilepsy en Synonym Active Case insensitive SNOMED CT core
2983928010 Myoclonic epilepsy myopathy sensory ataxia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2983952015 Myoclonic epilepsy myopathy sensory ataxia en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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