absent uvula Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of the uvula. (Human Phenotype Ontology, HP_0010292)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010292
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Genes

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

Symbol Name
ROR2 receptor tyrosine kinase-like orphan receptor 2