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Autosomal recessive spinocerebellar ataxia 11

MONDO:0013645

Any autosomal recessive syndromic cerebellar ataxia in which the cause of the disease is a mutation in the SYT14 gene.

Also known as: SCAR11, SYT14 autosomal recessive syndromic cerebellar ataxia, autosomal recessive spinocerebellar ataxia 11, autosomal recessive spinocerebellar ataxia type 11, autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14, spinocerebellar ataxia, autosomal recessive type 11, autosomal recessive cerebellar ataxia-psychomotor retardation syndrome, spinocerebellar ataxia, autosomal recessive 11

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

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Broader categories

Disease (618) 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) Inherited neurodegenerative disorder (10)
Trials to join now! 15 Not yet recruiting 3 Not yet finished but already full! 4 Completed 7
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