Autosomal recessive hereditary disorder	Congenital neurological disorder	Depletion of mitochondrial DNA	Hereditary cerebellar degeneration	Inherited metabolic disorder of nervous system	Spinocerebellar disease
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Myoclonic epilepsy myopathy sensory ataxia (disorder)
	Myoclonic epilepsy myopathy sensory ataxia
	Spinocerebellar ataxia with epilepsy MEMSA - myoclonic epilepsy myopathy sensory ataxia
	myoclonic epilepsy myopathy sensory ataxia
	MEMSA

Id	699328003
Status	Primitive

Occurrence

Associated morphology	Degenerative abnormality
Finding site	Spinal cord structure

Associated morphology	Degenerative abnormality
Finding site	Cerebellar structure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G11.9
Rule	TRUE
Advice	ALWAYS G11.9
Correlation	SNOMED CT source code to target map code correlation not specified

Target	G40.3
Rule	TRUE
Advice	ALWAYS G40.3
Correlation	SNOMED CT source code to target map code correlation not specified