Spinocerebellar Ataxia, Autosomal Recessive 26; Scar26
Genes related to Spinocerebellar Ataxia, Autosomal Recessive 26; Scar26
- XRCC1
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.
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.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 % |
You can get up to -5 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SCHNECKENBECKEN DYSPLASIA; SHNKND DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1 ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1 GABRIELE-DE VRIES SYNDROME; GADEVS PROLIDASE DEFICIENCY ATAXIA-OCULOMOTOR APRAXIA 4; AOA4 CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR