vocal cord paralysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A loss of the ability to move the vocal folds. (Human Phenotype Ontology, HP_0001605)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001605
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Genes

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

Symbol Name
DCTN1 dynactin 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
PMP22 peripheral myelin protein 22
SDHAF2 succinate dehydrogenase complex assembly factor 2
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3