spinocerebellar ataxia type 12
Human disease
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spinocerebellar ataxia type 12
Summary
spinocerebellar ataxia type 12 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 12's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 12's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 12's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 12 is a type of spinocerebellar ataxia[5].
- spinocerebellar ataxia type 12 is a type of autosomal dominant cerebellar ataxia type I[6].
- spinocerebellar ataxia type 12's NCI Thesaurus ID is recorded as C154316[7].
- spinocerebellar ataxia type 12's genetic association is recorded as PPP2R2B[8].
- spinocerebellar ataxia type 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050962[9].
- spinocerebellar ataxia type 12's exact match is recorded as http://identifiers.org/doid/DOID:0050962[10].
- spinocerebellar ataxia type 12's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98762[11].
- spinocerebellar ataxia type 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].