autosomal recessive spinocerebellar ataxia 13
Human disease
Press Enter · cited answer in seconds
0 sources
autosomal recessive spinocerebellar ataxia 13
Summary
autosomal recessive spinocerebellar ataxia 13 is a rare disease[1].
Key Facts
- autosomal recessive spinocerebellar ataxia 13's instance of is recorded as rare disease[2].
- autosomal recessive spinocerebellar ataxia 13's instance of is recorded as class of disease[3].
- autosomal recessive spinocerebellar ataxia 13 is a type of autosomal recessive cerebellar ataxia[4].
- autosomal recessive spinocerebellar ataxia 13 is a type of autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome[5].
- autosomal recessive spinocerebellar ataxia 13's genetic association is recorded as GRM1[6].
- autosomal recessive spinocerebellar ataxia 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080062[7].
- autosomal recessive spinocerebellar ataxia 13's exact match is recorded as http://identifiers.org/doid/DOID:0080062[8].
- autosomal recessive spinocerebellar ataxia 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_324262[9].
- autosomal recessive spinocerebellar ataxia 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_363429[10].
- autosomal recessive spinocerebellar ataxia 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].