laryngeal dystonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A focal dystonia that involves the muscles that control the vocal cords, resulting in strained or breathy speech. (Human Disease Ontology, DOID_0050844)
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4 genes associated with the laryngeal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FTL ferritin, light polypeptide
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
THAP1 THAP domain containing, apoptosis associated protein 1