|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050429)|
|Downloads & Tools|
1 genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
|ATP2C1||ATPase, Ca++ transporting, type 2C, member 1||2.88009|