Acquired Angioedema Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Acquired angioedema (AAE) is characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain due to an acquired C1 inhibitor (C1-INH) deficiency. (Orphanet Rare Disease Ontology, Orphanet_91385)
External Link https://www.disgenet.org/browser/0/1/0/C2931758
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Genes

4 genes associated with the disease Acquired Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
KNG1 kininogen 1
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1