Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Autosomal_recessive_cerebellar_ataxia> ?p ?o }
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- Autosomal_recessive_cerebellar_ataxia abstract "Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement. Signs and symptoms of the disorder first appear in early to mid-adulthood. People with this condition initially experience impaired speech (dysarthria), problems with coordination and balance (ataxia), or both. They may also have difficulty with movements that involve judging distance or scale (dysmetria). Other features of ARCA1 include abnormal eye movements (nystagmus) and problems following the movements of objects with their eyes. The movement problems are slowly progressive, often resulting in the need for a cane, walker, or wheelchair.".
- Autosomal_recessive_cerebellar_ataxia wikiPageExternalLink autosomal-recessive-cerebellar-ataxia-type-1.
- Autosomal_recessive_cerebellar_ataxia wikiPageExternalLink OC_Exp.php?Lng=EN&Expert=1172.
- Autosomal_recessive_cerebellar_ataxia wikiPageID "37750871".
- Autosomal_recessive_cerebellar_ataxia wikiPageLength "6035".
- Autosomal_recessive_cerebellar_ataxia wikiPageOutDegree "19".
- Autosomal_recessive_cerebellar_ataxia wikiPageRevisionID "664591943".
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink ARCA1.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Ataxia.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Category:Cerebellum.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Category:Neurological_disorders.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Category:Symptoms_and_signs:_Nervous_system.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Cerebellum.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Dysarthria.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Dysmetria.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Electrophysiology.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Enaptin.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Magnetic_resonance_imaging.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Molecular_Genetic_Testing.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Polyneurotherapy.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Prenatal_diagnosis.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Purkinje_cell.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Syne-1.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLink Teleangiectasias.
- Autosomal_recessive_cerebellar_ataxia wikiPageWikiLinkText "Autosomal recessive cerebellar ataxia".
- Autosomal_recessive_cerebellar_ataxia wikiPageUsesTemplate Template:Empty_section.
- Autosomal_recessive_cerebellar_ataxia wikiPageUsesTemplate Template:NLM_content.
- Autosomal_recessive_cerebellar_ataxia wikiPageUsesTemplate Template:Reflist.
- Autosomal_recessive_cerebellar_ataxia subject Category:Cerebellum.
- Autosomal_recessive_cerebellar_ataxia subject Category:Neurological_disorders.
- Autosomal_recessive_cerebellar_ataxia subject Category:Symptoms_and_signs:_Nervous_system.
- Autosomal_recessive_cerebellar_ataxia hypernym Condition.
- Autosomal_recessive_cerebellar_ataxia type Disease.
- Autosomal_recessive_cerebellar_ataxia type Disorder.
- Autosomal_recessive_cerebellar_ataxia type Institute.
- Autosomal_recessive_cerebellar_ataxia type Sign.
- Autosomal_recessive_cerebellar_ataxia type Source.
- Autosomal_recessive_cerebellar_ataxia comment "Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement. Signs and symptoms of the disorder first appear in early to mid-adulthood. People with this condition initially experience impaired speech (dysarthria), problems with coordination and balance (ataxia), or both. They may also have difficulty with movements that involve judging distance or scale (dysmetria).".
- Autosomal_recessive_cerebellar_ataxia label "Autosomal recessive cerebellar ataxia".
- Autosomal_recessive_cerebellar_ataxia sameAs Q4826996.
- Autosomal_recessive_cerebellar_ataxia sameAs m.0ngtf6y.
- Autosomal_recessive_cerebellar_ataxia sameAs Q4826996.
- Autosomal_recessive_cerebellar_ataxia wasDerivedFrom Autosomal_recessive_cerebellar_ataxia?oldid=664591943.
- Autosomal_recessive_cerebellar_ataxia isPrimaryTopicOf Autosomal_recessive_cerebellar_ataxia.