biliary cirrhosis Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	liver damage to parenchymal cells due to obstruction of bile flow in the bile ducts (Mammalian Phenotype Ontology, MP_0003256)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0002613
Similar Terms
Downloads & Tools

Genes

5 genes associated with the biliary cirrhosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ATP8B1	ATPase, aminophospholipid transporter, class I, type 8B, member 1
CFTR	cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CIRH1A	cirrhosis, autosomal recessive 1A (cirhin)
LBR	lamin B receptor
NPHP3	nephronophthisis 3 (adolescent)