Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 168507
Gene Symbol: PKD1L1
PKD1L1
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		0.310 GermlineCausalMutation ORPHANET Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans. 27616478

2016