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, 0 tagged with Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin itself.
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Browse by category →Sub-types of Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin
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TPM2-related myopathy 1 trial · 3 incl. sub-types
2 sub-types
- Central core myopathy 2 trials
- Congenital myopathy 23 0 trials
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Childhood-onset nemaline myopathy 1 trial · 2 incl. sub-types
6 sub-types
- Nemaline myopathy 6 1 trial
- Congenital myopathy 23 0 trials
- Congenital myopathy 2a, typical, autosomal dominant 0 trials
- Congenital myopathy 4B, autosomal recessive 0 trials
- Nemaline myopathy 2 0 trials
- Nemaline myopathy 9 0 trials
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TPM3-related myopathy 1 trial
3 sub-types
- Cap myopathy 0 trials
- Congenital myopathy 4A, autosomal dominant 0 trials
- Congenital myopathy 4B, autosomal recessive 0 trials
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Intermediate nemaline myopathy 0 trials
4 sub-types
- Congenital myopathy 2a, typical, autosomal dominant 0 trials
- Congenital myopathy 4B, autosomal recessive 0 trials
- Nemaline myopathy 2 0 trials
- Nemaline myopathy 9 0 trials
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Typical nemaline myopathy 0 trials
6 sub-types
- Congenital myopathy 23 0 trials
- Congenital myopathy 2a, typical, autosomal dominant 0 trials
- Nemaline myopathy 10 0 trials
- Nemaline myopathy 2 0 trials
- Nemaline myopathy 7 0 trials
- Nemaline myopathy 9 0 trials
Including sub-types (4)
Tagged with Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin (0)