Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/611174
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Genes

1 genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
IRX5 iroquois homeobox 5