Abortive cerebellar ataxia (disorder) {66988006 , SNOMED-CT } Acute cerebellar ataxia caused by varicella (disorder) {24059009 , SNOMED-CT } Acute cerebellar ataxia of childhood (disorder) {434311000124104 , SNOMED-CT } Ataxia pancytopenia syndrome (disorder) {768556005 , SNOMED-CT } Ataxia with deafness and intellectual disability syndrome (disorder) {720517001 , SNOMED-CT } Ataxia with tapetoretinal degeneration syndrome (disorder) {783203003 , SNOMED-CT } Autosomal dominant cerebellar ataxia type 2 (disorder) {1156796002 , SNOMED-CT } Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) {722293005 , SNOMED-CT } Autosomal recessive ataxia due to ubiquinone deficiency (disorder) {725394006 , SNOMED-CT } Autosomal recessive cerebellar ataxia Beauce type (disorder) {725433003 , SNOMED-CT } Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder) {1237625002 , SNOMED-CT } Autosomal recessive cerebellar ataxia with late-onset spasticity (disorder) {763348005 , SNOMED-CT } Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder) {715366004 , SNOMED-CT } Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder) {725408001 , SNOMED-CT } Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome (disorder) {766814006 , SNOMED-CT } Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) {773498006 , SNOMED-CT } Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) {770898002 , SNOMED-CT } Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder) {763312008 , SNOMED-CT } Autosomal recessive spastic ataxia with leukoencephalopathy (disorder) {784343003 , SNOMED-CT } Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome (disorder) {784347002 , SNOMED-CT } Cerebellar ataxia associated with another disorder (disorder) {192874000 , SNOMED-CT } Cerebellar ataxia caused by chemical (disorder) {1268825008 , SNOMED-CT } Cerebellar ataxia caused by toxin (disorder) {230243002 , SNOMED-CT } Cerebellar ataxia Cayman type (disorder) {717332007 , SNOMED-CT } Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder) {715371006 , SNOMED-CT } Cerebellar ataxia due to alcoholism (disorder) {361272001 , SNOMED-CT } Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder) {715984007 , SNOMED-CT } Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (disorder) {1236804009 , SNOMED-CT } Cerebellar ataxia with oculomotor apraxia type 4 (disorder) {1217230002 , SNOMED-CT } Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder) {763344007 , SNOMED-CT } Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) {1177169004 , SNOMED-CT } Dentatorubropallidoluysian degeneration (disorder) {68116008 , SNOMED-CT } Drug-induced cerebellar ataxia (disorder) {230242007 , SNOMED-CT } Dysequilibrium syndrome (disorder) {230782004 , SNOMED-CT } Dyssynergia cerebellaris myoclonica (disorder) {73495003 , SNOMED-CT } Early onset cerebellar ataxia (disorder) {230227009 , SNOMED-CT } Episodic ataxia (disorder) {421455009 , SNOMED-CT } Episodic ataxia type 3 (disorder) {718755009 , SNOMED-CT } Episodic ataxia type 4 (disorder) {718754008 , SNOMED-CT } Episodic ataxia type 5 (disorder) {718756005 , SNOMED-CT } Episodic ataxia type 6 (disorder) {718753002 , SNOMED-CT } Episodic ataxia type 7 (disorder) {718752007 , SNOMED-CT } Fragile X associated tremor ataxia syndrome (disorder) {448045004 , SNOMED-CT } Friedreich ataxia (disorder) {10394003 , SNOMED-CT } Gemignani syndrome (disorder) {782690007 , SNOMED-CT } Gillespie syndrome (disorder) {253176002 , SNOMED-CT } Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) {724283004 , SNOMED-CT } Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) {721846006 , SNOMED-CT } Infantile-onset autosomal recessive non progressive cerebellar ataxia (disorder) {785300001 , SNOMED-CT } Late onset cerebellar ataxia (disorder) {230232005 , SNOMED-CT } Leukoencephalopathy with mild cerebellar ataxia and white matter edema (disorder) {768663003 , SNOMED-CT } Marie's cerebellar ataxia (disorder) {46808003 , SNOMED-CT } Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder) {1237514002 , SNOMED-CT } Myoclonus, cerebellar ataxia, deafness syndrome (disorder) {733065003 , SNOMED-CT } Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (disorder) {1303586006 , SNOMED-CT } Non-progressive cerebellar ataxia with intellectual disability (disorder) {723441001 , SNOMED-CT } Nothnagel's syndrome (disorder) {32680009 , SNOMED-CT } Olivopontocerebellar degeneration (disorder) {67761004 , SNOMED-CT } Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) {1237413006 , SNOMED-CT } Progressive spinocerebellar ataxia with retained tendon reflexes (disorder) {230238009 , SNOMED-CT } Saldino-Mainzer dysplasia (disorder) {254092004 , SNOMED-CT } Sanger-Brown cerebellar ataxia (disorder) {37960002 , SNOMED-CT } Spinocerebellar ataxia (disorder) {129609000 , SNOMED-CT } Sporadic adult-onset ataxia of unknown etiology (disorder) {734023003 , SNOMED-CT } X-linked intellectual developmental disorder Christianson type (disorder) {702354007 , SNOMED-CT } X-linked intellectual disability with ataxia and apraxia syndrome (disorder) {718845002 , SNOMED-CT } X-linked non progressive cerebellar ataxia (disorder) {766818009 , SNOMED-CT } X-linked progressive cerebellar ataxia (disorder) {827172005 , SNOMED-CT }