Item 1 of 1 (back to results)   Spinocerebellar ataxia, autosomal recessive 6 C537312

Current search: C10. Nervous System Diseases: Nervous System Diseases [MESH:D009422] > Central Nervous System Diseases [MESH:D002493] > Spinal Cord Diseases [MESH:D013118] > Spinocerebellar Degenerations [MESH:D013132] > Spinocerebellar ataxia, autosomal recessive 6 [MESH:C537312] × Select any link to see items in a related category. more general categories    information about this item 4. Semantic Terms  4. Semantic Terms  Event [STY:T051] (3319)   Phenomenon or Process [STY:T067] (2498)   Natural Phenomenon or Process [STY:T070] (2415)   Biologic Function [STY:T038] (2363)   Pathologic Function [STY:T046] (2157)   Disease or Syndrome [STY:T047] (2055) C10. Nervous System Diseases  C10. Nervous System Diseases  Nervous System Diseases [MESH:D009422] (13325)   Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Cerebellar Diseases [MESH:D002526] (736)   Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 6 [MESH:C537312] (1)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 6 [MESH:C537312] (1)  Neurodegenerative Diseases [MESH:D019636] (6613)   Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 6 [MESH:C537312] (1) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Genetic Diseases, Inborn [MESH:D030342] (9766)   Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 6 [MESH:C537312] (1)