| 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 |
| Similar Terms | |
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1 genes associated with the nasopharyngeal carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TP53 | tumor protein p53 |