Hereditary cerebellar degeneration

Hereditary cerebellar degeneration (disorder)

active

Code	`37650008`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20020131

Parents (2)

95646004Cerebellar degeneration disorder
106018006Hereditary degenerative disease of central nervous system disorder

Children (16)

722293005Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome disorder
1237625002Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency disorder
770898002Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency disorder
1172843003Combined oxidative phosphorylation defect type 29 disorder
782737003Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome disorder
10394003Friedreich ataxia disorder
1172696009Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome disorder
724283004Hypomyelinating leucodystrophy with atrophy of basal ganglia and cerebellum disorder
782822006Infantile cerebellar and retinal degeneration disorder
770725000Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly disorder
1237514002Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome disorder
699328003Myoclonic epilepsy myopathy sensory ataxia disorder
1217381009Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome disorder
1373775000Neuronal ceroid lipofuscinosis type 11 disorder
1208481000Progressive cerebello-cerebral atrophy disorder
129609000Spinocerebellar ataxia disorder