RS149033995 FKTN
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Associated Conditions
Walker-Warburg congenital muscular dystrophy
Dilated cardiomyopathy 1X
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
type B4
type A
4
Autosomal recessive limb-girdle muscular dystrophy type 2M
Cardiovascular phenotype
Walker-Warburg congenital muscular dystrophy
Dilated cardiomyopathy 1X
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
Other Variants in FKTN