dyskinetic 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 extrapyramidal motor system and/or pyramidal tract and to the basal ganglia, which results in mixed muscle tone (hypertonia and hypotonia). The individuals have trouble holding themselves in an upright, steady position for sitting or walking, and often show involuntary motions. (Human Disease Ontology, DOID_0050672)
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6 genes co-occuring with the disease dyskinetic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
OR10K2 olfactory receptor, family 10, subfamily K, member 2 1.12108
HPRT1 hypoxanthine phosphoribosyltransferase 1 0.921323
PIDD1 p53-induced death domain protein 1 0.899103
MNX1 motor neuron and pancreas homeobox 1 0.8741
NKX2-1 NK2 homeobox 1 0.861818
NPHS1 nephrosis 1, congenital, Finnish type (nephrin) 0.846669