generalized dystonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A dystonia that affects most or all of the body. (Human Disease Ontology, DOID_0050835)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007325
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Genes

3 genes associated with the generalized dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
SUOX sulfite oxidase
TUBB4A tubulin, beta 4A class IVa