mastoiditis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A middle ear disease characterized by an inflammation of the mucosal lining of the mastoid antrum and the mastoid air cell system inside the mastoid process. (Human Disease Ontology, DOID_0060322)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000265
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Genes

3 genes associated with the mastoiditis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NBN nibrin
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2