Searched for "Myopathies, Structural, Congenital".
15
results
found
on Genetics Home Reference.
- centronuclear myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- X-linked myotubular myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- actin-accumulation myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- Bethlem myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- cap myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- central core disease condition summary
Related classification: Myopathies, Structural, Congenital
- congenital fiber-type disproportion condition summary
Related classification: Myopathies, Structural, Congenital
- intranuclear rod myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- myofibrillar myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- nemaline myopathy condition summary
Related classification: Myopathies, Structural, Congenital
- BIN1 gene summary
Official name: bridging integrator 1
Found related term: ...gene have been found to cause centronuclear myopathy. Most of these mutations change...
- DNM2 gene summary
Official name: dynamin 2
Found related term: ...gene have been found to cause centronuclear myopathy. Most of these mutations change...
- MTM1 gene summary
Official name: myotubularin 1
Found related term in link title: X-Linked Centronuclear Myopathy
- MYF6 gene information
Official name: myogenic factor 6 (herculin)
Found related term: ...a cause of autosomal dominant centronuclear myopathy (ADCNM). [provided by RefSeq, May...
- MTMR14 gene information
Official name: myotubularin related protein 14
Found related term: ...with autosomal dominant centronuclear myopathy. Alternate splicing results in...
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