progressive weakness
Basic Information
- Identifier
- SYMP_0000363
- Notation
- SYMP:0000363
- Category
- symptoms
Related Diseases
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- amyotrophic lateral sclerosis type 6
- autosomal dominant distal hereditary motor neuronopathy 9
- autosomal dominant limb-girdle muscular dystrophy type 2
- autosomal recessive distal hereditary motor neuronopathy 4
- autosomal recessive distal hereditary motor neuronopathy 5
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- centronuclear myopathy 1
- congenital muscular dystrophy
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- congenital myasthenic syndrome 14
- congenital myasthenic syndrome 1A
- congenital myasthenic syndrome 1B
- congenital myasthenic syndrome 2A
- congenital myasthenic syndrome 3A
- congenital myasthenic syndrome 3B
- congenital myasthenic syndrome 4A
- congenital myasthenic syndrome 4B
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- hereditary spastic paraplegia 8
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- myofibrillar myopathy 9
- nemaline myopathy 11
- nemaline myopathy 6
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- spinal muscular atrophy
- spondyloepiphyseal dysplasia Maroteaux type
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