bilateral radial aplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Missing radius bone on both sides associated with congenital failure of development. (Human Phenotype Ontology, HP_0004977)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004977
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Genes

1 genes associated with the bilateral radial aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
RBM8A RNA binding motif protein 8A