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- Brown-Vialetto-Van Laere syndrome condition summary
Found in link title: Neuromuscular Disorders
- congenital myasthenic syndrome condition summary
Found in link title: Neuromuscular Disorders
- distal hereditary motor neuropathy, type II condition summary
Found in link title: Neuromuscular Disorders
- distal hereditary motor neuropathy, type V condition summary
Found in link title: Neuromuscular Disorders
- L1 syndrome condition summary
Found in link title: Neuromuscular Disorders
- mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes condition summary
Found in link title: Neuromuscular Disorders
Related genes and chromosomes:
- Silver syndrome condition summary
Found in link title: Neuromuscular Disorders
- spastic paraplegia type 11 condition summary
Found in link title: Neuromuscular Disorders
- spastic paraplegia type 2 condition summary
Found in link title: Neuromuscular Disorders
- spastic paraplegia type 3A condition summary
Found in link title: Neuromuscular Disorders
- spastic paraplegia type 4 condition summary
Found in link title: Neuromuscular Disorders
- spastic paraplegia type 7 condition summary
Found in link title: Neuromuscular Disorders
- spastic paraplegia type 8 condition summary
Found in link title: Neuromuscular Disorders
- Troyer syndrome condition summary
Found in link title: Neuromuscular Disorders
- ataxia with vitamin E deficiency condition summary
Found in link title: Neuromuscular Disorders
- Christianson syndrome condition summary
Found in link title: Neuromuscular Disorders
- hereditary hyperekplexia condition summary
Found in link title: Neuromuscular Disorders
- multiple pterygium syndrome condition summary
Found in link title: Neuromuscular Disorders
- Pelizaeus-Merzbacher disease condition summary
Found in link title: Neuromuscular Disorders
- actin-accumulation myopathy condition summary
Related classification: Neuromuscular Diseases