Neuromuscular disease caused by qualitative or quantitative defects of titin
MONDO:0016191Also known as: qualitative or quantitative defects of titin
4 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
TTN-related myopathy
(2)
Autosomal recessive limb-girdle muscular dystrophy type 2J
(1)
Early-onset myopathy with fatal cardiomyopathy
(1)
Autosomal dominant titinopathy
(0)
Autosomal recessive centronuclear myopathy
(0)
Autosomal recessive distal titinopathy
(0)
Autosomal recessive titinopathy
(0)
Classic multiminicore myopathy
(0)
Dilated cardiomyopathy 1G
(0)
Emery-Dreifuss-like muscular dystrophy
(0)
Hypertrophic cardiomyopathy 9
(0)
Myopathy, centronuclear, 2
(0)
Myopathy, centronuclear, 5
(0)
Myopathy, myofibrillar, 9, with early respiratory failure
(0)
Tibial muscular dystrophy
(0)
Titinopathy with congenital contractures
(0)