Vocal Cord Paralysis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A loss of the ability to move the vocal folds. (Human Phenotype Ontology, HP_0001605)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014826
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1 genes/proteins associated with the disease Vocal Cord Paralysis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.09786