Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115399
Gene Symbol: LRRC56
LRRC56
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.300 GermlineCausalMutation ORPHANET Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects. 30388400

2018