congenital fibrosis of the extraocular muscles Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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Genes

1 genes associated with the disease congenital fibrosis of the extraocular muscles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
KIF21A kinesin family member 21A