Disease: Hepatic Fibrosis, Congenital ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatic Fibrosis, Congenital
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
0.700 CausalMutation CLINVAR Contribution of the TTC21B gene to glomerular and cystic kidney diseases. 26940125 2017
Hepatic Fibrosis, Congenital
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
0.700 CausalMutation CLINVAR A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. 24876116 2014