spinocerebellar ataxia type 7
Human disease
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Summary
spinocerebellar ataxia type 7 is a developmental defect during embryogenesis[1]. It is known by 13 alternative names across languages and contexts.[2]
Key Facts
- spinocerebellar ataxia type 7's instance of is recorded as developmental defect during embryogenesis[3].
- spinocerebellar ataxia type 7's instance of is recorded as rare disease[4].
- spinocerebellar ataxia type 7's instance of is recorded as class of disease[5].
- spinocerebellar ataxia type 7 is a type of spinocerebellar ataxia[6].
- spinocerebellar ataxia type 7 is a type of autosomal dominant cerebellar ataxia type II[7].
- spinocerebellar ataxia type 7's NCI Thesaurus ID is recorded as C126562[8].
- spinocerebellar ataxia type 7's genetic association is recorded as ATXN7[9].
- spinocerebellar ataxia type 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050958[10].
- spinocerebellar ataxia type 7's exact match is recorded as http://identifiers.org/doid/DOID:0050958[11].
- spinocerebellar ataxia type 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_94147[12].
- spinocerebellar ataxia type 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
spinocerebellar ataxia type 7 is known by 13 alternative names across languages and contexts.[2]