abnormality of the mastoid Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the mastoid process, which is the conical prominence projecting from the undersurface of the mastoid portion of the temporal bone. (Human Phenotype Ontology, HP_0000264)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000264
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Genes

3 genes associated with the abnormality of the mastoid 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