congenital fibrosis of extraocular muscles Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital non-progressive ophthalmoplegia with multiple extraocular muscle restrictions. Typically, there is ptosis and variable degrees of restriction of horizontal and vertical eye movements. (Human Phenotype Ontology, HP_0001491)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001491
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Genes

4 genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KIF21A kinesin family member 21A
PHOX2A paired-like homeobox 2a
TUBB2B tubulin, beta 2B class IIb
TUBB3 tubulin, beta 3 class III