spinocerebellar ataxia type 35
Human disease
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spinocerebellar ataxia type 35
Summary
spinocerebellar ataxia type 35 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 35's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 35's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 35's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 35 is a type of spinocerebellar ataxia[5].
- spinocerebellar ataxia type 35 is a type of autosomal dominant cerebellar ataxia type I[6].
- spinocerebellar ataxia type 35's genetic association is recorded as TGM6[7].
- spinocerebellar ataxia type 35's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050982[8].
- spinocerebellar ataxia type 35's exact match is recorded as http://identifiers.org/doid/DOID:0050982[9].
- spinocerebellar ataxia type 35's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_276193[10].
- spinocerebellar ataxia type 35's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].