|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormal accumulation of fluid leading to swelling of the pharynx. (Human Phenotype Ontology, HP_0011855)|
|Downloads & Tools|
1 genes associated with the pharyngeal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SERPING1||serpin peptidase inhibitor, clade G (C1 inhibitor), member 1|