bifid ribs Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bifid rib refers to cleavage of the sternal end of a rib, usually unilateral. Bifid ribs are usually asymptomatic, and are often discovered incidentally by chest x-ray. (Human Phenotype Ontology, HP_0000892)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000892
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Genes

4 genes associated with the bifid ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PTCH1 patched 1
PTCH2 patched 2
SUFU suppressor of fused homolog (Drosophila)
TMCO1 transmembrane and coiled-coil domains 1