oculomotor apraxia, congenital, cogan-type Gene Set

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

1 genes associated with the oculomotor apraxia, congenital, cogan-type phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
COMA Cogan-type congential oculomotor apraxia