spinocerebellar ataxia type 17
Human disease
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spinocerebellar ataxia type 17
Summary
spinocerebellar ataxia type 17 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 17's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 17's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 17's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 17 is a type of spinocerebellar ataxia[5].
- spinocerebellar ataxia type 17 is a type of autosomal dominant cerebellar ataxia type I[6].
- spinocerebellar ataxia type 17 is a type of Huntington's disease-like syndrome[7].
- spinocerebellar ataxia type 17 is a type of miscellaneous movement disorder due to genetic neurodegenerative disease[8].
- spinocerebellar ataxia type 17's NCI Thesaurus ID is recorded as C179861[9].
- spinocerebellar ataxia type 17's genetic association is recorded as TBP[10].
- spinocerebellar ataxia type 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050967[11].
- spinocerebellar ataxia type 17's exact match is recorded as http://identifiers.org/doid/DOID:0050967[12].
- spinocerebellar ataxia type 17's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98759[13].
- spinocerebellar ataxia type 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].