Acquired angioedema Gene Set

Dataset CTD 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 http://ctdbase.org/detail.go?type=disease&acc=MESH:C538173
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Genes

2 genes/proteins associated with the disease Acquired angioedema from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KNG1 kininogen 1 2.88009
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1 2.88009