absent in utero rib ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of formation and mineralization of the ribs in utero. (Human Phenotype Ontology, HP_0006615)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006615
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Genes

1 genes associated with the absent in utero rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator