Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2218
Gene Symbol: FKTN
FKTN
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		0.660 GermlineCausalMutation ORPHANET This is the first time a mutation localized outside of the fukutin coding region has been identified as a cause of WWS. 18177472

2008
Entrez Id: 2218
Gene Symbol: FKTN
FKTN
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		0.660 GermlineCausalMutation ORPHANET Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. 17878207

2007