aplasia of the inner ear Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the inner ear due to a developmental defect. (Human Phenotype Ontology, HP_0011372)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011372
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1 genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGF3 fibroblast growth factor 3