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Results 1 - 5 of 5 for Autosomal recessive spinocerebellar ataxia 7
  1. TPP1 gene 
    ... JT, van de Warrenburg BP, Maat-Kievit AJ. Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  2. Infantile-onset spinocerebellar ataxia 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... PubMed Finsterer J. Ataxias with ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  3. Primary coenzyme Q10 deficiency 
    ... PDSS1 PDSS2 This condition is inherited in an autosomal recessive pattern, which means both copies of a gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  4. Ataxia with oculomotor apraxia 
    ... types of this condition are inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  5. Huntington's disease-like 
    ... the gene. HDL3 is probably inherited in an autosomal recessive pattern, which means both copies of the gene ... disorder. The parents of an individual with an autosomal recessive condition each carry one copy of the altered ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease-like - Genetics