spinocerebellar ataxia, autosomal recessive 25
human disease
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spinocerebellar ataxia, autosomal recessive 25
Summary
spinocerebellar ataxia, autosomal recessive 25 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia, autosomal recessive 25's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia, autosomal recessive 25's instance of is recorded as class of disease[3].
- spinocerebellar ataxia, autosomal recessive 25 is a type of autosomal recessive cerebellar ataxia[4].
- spinocerebellar ataxia, autosomal recessive 25's genetic association is recorded as ATG5[5].
- spinocerebellar ataxia, autosomal recessive 25's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080259[6].
- spinocerebellar ataxia, autosomal recessive 25's exact match is recorded as http://identifiers.org/doid/DOID:0080259[7].
- spinocerebellar ataxia, autosomal recessive 25's on focus list of Wikimedia project is recorded as WikiProject Medicine[8].