nasopharyngeal carcinoma Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pharynx cancer that is located_in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract. (Human Disease Ontology, DOID_9261)
External Link http://www.omim.org/entry/607107
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Genes

1 genes associated with the nasopharyngeal carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TP53 tumor protein p53