ophthalmoparesis Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description Ophthalmoplegia is a paralysis or weakness of one or more of the muscles that control eye movement. (Human Phenotype Ontology, HP_0000597)
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Genes

4 genes co-occuring with the biological term ophthalmoparesis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
LARS leucyl-tRNA synthetase
POLG polymerase (DNA directed), gamma
RYR1 ryanodine receptor 1 (skeletal)