Cerebellar degeneration
Hereditary degenerative disease of central nervous system
||
Hereditary cerebellar degeneration (disorder)
Hereditary cerebellar degeneration
hereditaire cerebellaire degeneratie
Id37650008
StatusDefined
Associated morphologyDegenerative abnormality
Finding siteCerebellar structure
ICD-10 complex map reference set
TargetG11.9
RuleTRUE
AdviceALWAYS G11.9
CorrelationSNOMED CT source code to target map code correlation not specified
|
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Combined oxidative phosphorylation defect type 29
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
Infantile cerebellar and retinal degeneration
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Myoclonic epilepsy myopathy sensory ataxia
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
Progressive cerebello-cerebral atrophy
Spinocerebellar ataxia57