Alagille Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts. (Human Disease Ontology, DOID_9245)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D016738
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Genes

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

Symbol Name Standardized Value
NOTCH2 notch 2 2.88009
JAG1 jagged 1 2.88009