writer's cramp Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A focal dystonia of the fingers, hand, and/or forearm that appears when the affected person attempts to do a task that requires fine motor movements such as writing or playing a musical instrument. (Human Phenotype Ontology, HP_0002356)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002356
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Genes

6 genes associated with the writer's cramp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DRD2 dopamine receptor D2
FTL ferritin, light polypeptide
GCH1 GTP cyclohydrolase 1
SGCE sarcoglycan, epsilon
THAP1 THAP domain containing, apoptosis associated protein 1
TOR1A torsin family 1, member A (torsin A)