Spinocerebellar Ataxia, Autosomal Recessive 26; Scar26

Clinical Features

Top most frequent phenotypes and symptoms related to Spinocerebellar Ataxia, Autosomal Recessive 26; Scar26

  • Ataxia
  • Nystagmus
  • Muscle weakness
  • Peripheral neuropathy
  • Dysarthria
  • Dysphagia
  • Cerebellar atrophy
  • Areflexia
  • Distal muscle weakness
  • Dysmetria

And another 11 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


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Spinocerebellar Ataxia, Autosomal Recessive 26; Scar26 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
XRCC1.

By Fulgent Genetics Fulgent Genetics (United States).

XRCC1
Specificity
100 %
Genes
100 %
152 Integrated Advantage NGS Solid Tumor Panel.

By Integrated Molecular Diagnostics Pathology, Inc. (United States).

ROS1, RRM1, SLCO1B1, BRAF, BRCA1, SLC29A1, BRCA2, SMO, SPARC, SRC, STAT3, STK11, AURKB, AURKA, SULT1A1, SYK, TGFBR2, TNFAIP3, MED12, TOP1 , (...)

View the complete list with 129 more genes
Specificity
1 %
Genes
100 %
Tempus xT assay.

By Tempus Labs, Inc. (United States).

BCL6, RIT1, BCL7A, BCR, ROS1, RPL5, RPS15, RPS6KB1, RUNX1, RXRA, BLM, SDHA, SDHB, SDHC, SDHD, SEC23B, SEMA3C, BMPR1A, SF3B1, SRSF2 , (...)

View the complete list with 555 more genes
Specificity
1 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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