autosomal recessive spinocerebellar ataxia 18
Human disease
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autosomal recessive spinocerebellar ataxia 18
Summary
autosomal recessive spinocerebellar ataxia 18 is a rare disease[1].
Key Facts
- autosomal recessive spinocerebellar ataxia 18's instance of is recorded as rare disease[2].
- autosomal recessive spinocerebellar ataxia 18's instance of is recorded as class of disease[3].
- autosomal recessive spinocerebellar ataxia 18 is a type of autosomal recessive cerebellar ataxia[4].
- autosomal recessive spinocerebellar ataxia 18 is a type of autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome[5].
- autosomal recessive spinocerebellar ataxia 18's genetic association is recorded as GRID2[6].
- autosomal recessive spinocerebellar ataxia 18's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080042[7].
- autosomal recessive spinocerebellar ataxia 18's exact match is recorded as http://identifiers.org/doid/DOID:0080042[8].
- autosomal recessive spinocerebellar ataxia 18's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_363429[9].
- autosomal recessive spinocerebellar ataxia 18's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_363432[10].
- autosomal recessive spinocerebellar ataxia 18's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].