spinocerebellar ataxia type 6
Human disease
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spinocerebellar ataxia type 6
Summary
spinocerebellar ataxia type 6 is a developmental defect during embryogenesis[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- spinocerebellar ataxia type 6's instance of is recorded as developmental defect during embryogenesis[3].
- spinocerebellar ataxia type 6's instance of is recorded as rare disease[4].
- spinocerebellar ataxia type 6's instance of is recorded as class of disease[5].
- spinocerebellar ataxia type 6 is a type of spinocerebellar ataxia[6].
- spinocerebellar ataxia type 6 is a type of autosomal dominant cerebellar ataxia type III[7].
- spinocerebellar ataxia type 6's NCI Thesaurus ID is recorded as C142838[8].
- spinocerebellar ataxia type 6's health specialty is recorded as neurology[9].
- spinocerebellar ataxia type 6's genetic association is recorded as CACNA1A[10].
- spinocerebellar ataxia type 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050956[11].
- spinocerebellar ataxia type 6's exact match is recorded as http://identifiers.org/doid/DOID:0050956[12].
- spinocerebellar ataxia type 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
spinocerebellar ataxia type 6 is known by 6 alternative names across languages and contexts.[2]