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, 0 tagged with Neuromuscular disease caused by qualitative or quantitative defects of titin itself.
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Browse by category →Sub-types of Neuromuscular disease caused by qualitative or quantitative defects of titin
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TTN-related myopathy 2 trials · 4 incl. sub-types
2 sub-types
- Autosomal recessive titinopathy 0 trials · 2 incl. sub-types Sub-types →
- Autosomal dominant titinopathy 0 trials Sub-types →
Most studied deeper sub-types
Autosomal recessive limb-girdle muscular dystrophy type 2J
(1)
Early-onset myopathy with fatal cardiomyopathy
(1)
Autosomal recessive centronuclear myopathy
(0)
Autosomal recessive distal 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)
Including sub-types (4)
Tagged with Neuromuscular disease caused by qualitative or quantitative defects of titin (0)
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