TTC21B-AS1, TTC21B antisense RNA 1, 100506134

N. diseases: 11; N. variants: 6
Disease: Hepatic Fibrosis, Congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		0.100 CausalMutation disease CLINVAR Contribution of the TTC21B gene to glomerular and cystic kidney diseases. 26940125 2017
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		0.100 CausalMutation disease CLINVAR A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. 24876116 2014