ataxic cerebral palsy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A cerebral palsy that is caused by damage to the cerebellum, which affects muscle coordination, particularly in the limb. Some individuals suffer from hypotonia, tremors, difficulty with visual and/or auditory processing. (Human Disease Ontology, DOID_0050670)
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Genes

3 genes co-occuring with the disease ataxic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MCOLN1 mucolipin 1 1.35028
UBE3A ubiquitin protein ligase E3A 1.24863
GFAP glial fibrillary acidic protein 0.781888