RS374058726 TTN
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Associated Conditions
Inborn genetic diseases
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Myopathy
myofibrillar
9
with early respiratory failure
Cardiomyopathy
Early-onset myopathy with fatal cardiomyopathy
Tibial muscular dystrophy
Cardiovascular phenotype
TTN-related disorder
Inborn genetic diseases
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Other Variants in TTN