IGSF3, immunoglobulin superfamily member 3, 3321

N. diseases: 18; N. variants: 1
Disease: LACRIMAL DUCT DEFECT ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1835612
Disease: LACRIMAL DUCT DEFECT
LACRIMAL DUCT DEFECT 		0.400 GermlineCausalMutation phenotype ORPHANET Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. 24372406 2014
CUI: C1835612
Disease: LACRIMAL DUCT DEFECT
LACRIMAL DUCT DEFECT 		0.400 CausalMutation phenotype CLINVAR