|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes/proteins associated with the disease Acquired angioedema from the curated CTD Gene-Disease Associations dataset.