stapes ankylosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Stapes ankylosis refers to congenital or acquired fixation of the stapes (the stirrup-shaped small bone or ossicle in the middle ear), which is associated with conductive hearing resulting from impairment of the sound-conduction mechanism (the external auditory canal, tympanic membrane, and/or middle-ear ossicles). (Human Phenotype Ontology, HP_0000381)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000381
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Genes

2 genes associated with the stapes ankylosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NOG noggin
POU3F4 POU class 3 homeobox 4