| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Any abnormality of the parotid glands, which are the salivary glands that are located in the subcutaneous tissues of the face overlying the mandibular ramus and anterior and inferior to the external ear. (Human Phenotype Ontology, HP_0000197) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0000197 |
| Similar Terms | |
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6 genes associated with the abnormality of parotid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
