Myopathy caused by variation in FKTN

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Pathways column key: KEGG Reactome
Disease terms 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 →
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a4 1 shared geneFKTN Related via 1 shared gene including FKTN. Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type b4 1 shared geneFKTN Related via 1 shared gene including FKTN. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a 1 shared geneFKTN Related via 1 shared gene including FKTN. 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.