autosomal recessive spinocerebellar ataxia 12 (Q21124570)

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human disease
  • autosomal recessive spinocerebellar ataxia type 12
  • SCAR12
  • Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency
  • Spinocerebellar Ataxia With Mental Retardation and Epilepsy
  • SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12
  • Spinocerebellar Ataxia, Autosomal Recessive type 12
  • SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
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Language Label Description Also known as
English
autosomal recessive spinocerebellar ataxia 12
human disease
  • autosomal recessive spinocerebellar ataxia type 12
  • SCAR12
  • Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency
  • Spinocerebellar Ataxia With Mental Retardation and Epilepsy
  • SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12
  • Spinocerebellar Ataxia, Autosomal Recessive type 12
  • SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12

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