Pemphigus, Benign Familial Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050429)
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1 genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1 2.88009