spinocerebellar ataxia type 42
human disease
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spinocerebellar ataxia type 42
Summary
spinocerebellar ataxia type 42 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 42's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 42's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 42's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 42 is a type of autosomal dominant cerebellar ataxia type III[5].
- spinocerebellar ataxia type 42 is a type of spinocerebellar ataxia[6].
- spinocerebellar ataxia type 42's NCI Thesaurus ID is recorded as C171269[7].
- spinocerebellar ataxia type 42's genetic association is recorded as CACNA1G[8].
- spinocerebellar ataxia type 42's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_458803[9].
- spinocerebellar ataxia type 42's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111742[10].
- spinocerebellar ataxia type 42's exact match is recorded as http://identifiers.org/doid/DOID:0111742[11].