autosomal recessive spinocerebellar ataxia 12
human disease
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autosomal recessive spinocerebellar ataxia 12
Summary
autosomal recessive spinocerebellar ataxia 12 is a developmental defect during embryogenesis[1].
Key Facts
- autosomal recessive spinocerebellar ataxia 12's instance of is recorded as developmental defect during embryogenesis[2].
- autosomal recessive spinocerebellar ataxia 12's instance of is recorded as rare disease[3].
- autosomal recessive spinocerebellar ataxia 12's instance of is recorded as class of disease[4].
- autosomal recessive spinocerebellar ataxia 12 is a type of autosomal recessive cerebellar ataxia[5].
- autosomal recessive spinocerebellar ataxia 12 is a type of autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome[6].
- autosomal recessive spinocerebellar ataxia 12's genetic association is recorded as WWOX[7].
- autosomal recessive spinocerebellar ataxia 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080060[8].
- autosomal recessive spinocerebellar ataxia 12's exact match is recorded as http://identifiers.org/doid/DOID:0080060[9].
- autosomal recessive spinocerebellar ataxia 12's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_284282[10].
- autosomal recessive spinocerebellar ataxia 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].