TTC21B, tetratricopeptide repeat domain 21B, 79809

N. diseases: 76; N. variants: 24
Disease: NEPHRONOPHTHISIS 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1865872
Disease: NEPHRONOPHTHISIS 2
NEPHRONOPHTHISIS 2 		0.400 GermlineCausalMutation disease ORPHANET TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. 21258341 2011
CUI: C1865872
Disease: NEPHRONOPHTHISIS 2
NEPHRONOPHTHISIS 2 		0.400 CausalMutation disease CLINVAR