vocal cord paresis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased strength of the vocal folds. (Human Phenotype Ontology, HP_0001604)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001604
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Genes

6 genes associated with the vocal cord paresis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GDAP1 ganglioside induced differentiation associated protein 1
MFN2 mitofusin 2
PRX periaxin
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
SLC5A7 solute carrier family 5 (sodium/choline cotransporter), member 7
TRPV4 transient receptor potential cation channel, subfamily V, member 4