myopathy caused by variation in FKTN

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
myopathy caused by variation in FKTN
FKTN Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with myopathy caused by variation in FKTN.
5 View disease cluster →
Muscle eye brain disease 1 shared geneFKTN Related via 1 shared gene including FKTN. Walker-warburg syndrome 1 shared geneFKTN Related via 1 shared gene including FKTN. Congenital muscular dystrophy 1 shared geneFKTN Related via 1 shared gene including FKTN. Limb girdle muscular dystrophy 1 shared geneFKTN Related via 1 shared gene including FKTN. Muscular dystrophy 1 shared geneFKTN Related via 1 shared gene including FKTN.