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Autosomal recessive spinocerebellar ataxia 15

MONDO:0014311

Any autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome in which the cause of the disease is a mutation in the RUBCN gene.

Also known as: RUBCN autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome, RUBCN autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome, SCAR15, autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in RUBCN, autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in RUBCN, autosomal recessive spinocerebellar ataxia type 15, spinocerebellar ataxia, autosomal recessive type 15, Salih ataxia

33 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Epilepsy (398) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Brain disorder (110) Central nervous system disorder (97) Movement disorder (89) Cerebellar ataxia (32) Human disease (14)
Trials to join now! 18 Not yet recruiting 3 Not yet finished but already full! 5 Completed 7
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