spinocerebellar
31SDSEM — • spinocerebellar degeneration slow eye movements [syndrome] …
32SpnCbT — • spinocerebellar tract …
33tract — An elongated area, e.g., path, track, way. SEE ALSO: fascicle. SYN: tractus. [L. tractus, a drawing out] alimentary t. SYN: digestive t.. anterior corticospinal t. uncrossed fibers forming a small bundle in the anterior funiculus of the …
34Trinucleotide repeat disorder — Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation …
35ATXN2 — Ataxin 2, also known as ATXN2, is a human gene. PBB Summary section title = summary text = Mutations in ATXN2 cause spinocerebellar ataxia type 2 (SCA2). The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of… …
36Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH …
37Anterior corticospinal tract — seen in red at bottom center in figure (text tag found at upper left) …
38ATXN10 — Ataxin 10, also known as ATXN10, is a human gene.cite web | title = Entrez Gene: ATXN10 ataxin 10| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=25814| accessdate = ] PBB Summary section title = summary… …
39ATXN8OS — Ataxin 8 opposite strand, also known as ATXN8OS, is a human gene.cite web | title = Entrez Gene: ATXN8OS ataxin 8 opposite strand| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6315| accessdate = ] PBB… …
40nervous system disease — Introduction any of the diseases or disorders that affect the functioning of the human nervous system (nervous system, human). Everything that humans sense, consider, and effect and all the unlearned reflexes of the body depend on the… …
