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Disease Info Card
Biemond Ataxia
Information about Biemond Ataxia: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Biemond Ataxia
Most recent studies have shown that Biemond Ataxia shares some biological mechanisms with acquired-kyphosis, ataxia, friedreich-ataxia, gastric-ulcer, leukemia, leukemia-feline, neurodegenerative-disorders, neurologic-signs, retinitis-pigmentosa, scoliosis-unspecified, sensation-disorders, sensory-ataxia, sensory-neuropathy, spinal-cord-diseases, spinocerebellar-degeneration.
Among the many pathways, these few ones have gauged particular interests from scientists studying Biemond Ataxia, and have been seen in publications frequently: Heme Export, Localization, Pathogenesis, Proprioception
Quite a number of genes have been found to play important roles in Biemond Ataxia, such as ATN1, CRP, CSF2, CSRP1, EPYC, FLVCR1, GJB1, LAMC2, OGN, OPTC, PLEKHM1, PMP22, RHCE, RHD. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Biemond Ataxia
This information is being compiled and will come in a future update
| Heme Export | Localization | Pathogenesis |
| Proprioception |