Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin
MONDO:0017303Also known as: qualitative or quantitative defects of tropomyosin
4 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Central core myopathy
(2)
Childhood-onset nemaline myopathy
(1)
Nemaline myopathy 6
(1)
TPM2-related myopathy
(1)
TPM3-related myopathy
(1)
Cap myopathy
(0)
Congenital myopathy 23
(0)
Congenital myopathy 2a, typical, autosomal dominant
(0)
Congenital myopathy 4A, autosomal dominant
(0)
Congenital myopathy 4B, autosomal recessive
(0)
Intermediate nemaline myopathy
(0)
Nemaline myopathy 10
(0)
Nemaline myopathy 2
(0)
Nemaline myopathy 7
(0)
Nemaline myopathy 9
(0)
Typical nemaline myopathy
(0)