laryngeal edema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal accumulation of fluid and swelling in the tissues of the larynx. (Human Phenotype Ontology, HP_0012027)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012027
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Genes

1 genes associated with the laryngeal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1