progressive external ophthalmoplegia, autosomal dominant, 3 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/609286
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Genes

1 genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2