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Metadata
ID	SYMP:0000363
Name	progressive weakness
Parent Relationships	is_a weakness
Related Diseases	has symptom Gamstorp-Wohlfart syndrome adult spinal muscular atrophy intermediate spinal muscular atrophy congenital muscular dystrophy X-linked myopathy with excessive autophagy inclusion body myopathy with Paget disease of bone and frontotemporal dementia Troyer syndrome syndromic X-linked intellectual disability Chudley-Schwartz type Marinesco-Sjogren syndrome congenital muscular dystrophy with cataracts and intellectual disability myofibrillar myopathy myofibrillar myopathy 8 autosomal recessive limb-girdle muscular dystrophy type 2Z congenital myasthenic syndrome 1B congenital myasthenic syndrome 1A congenital myasthenic syndrome 3B congenital myasthenic syndrome 3A congenital myasthenic syndrome 14 congenital myasthenic syndrome 4B congenital myasthenic syndrome 4A congenital myasthenic syndrome 2A hereditary spastic paraplegia 4 hereditary spastic paraplegia 5A nemaline myopathy 11 nemaline myopathy 6 myofibrillar myopathy 9 autosomal dominant distal hereditary motor neuronopathy 9 autosomal recessive distal hereditary motor neuronopathy 4 autosomal recessive distal hereditary motor neuronopathy 5 centronuclear myopathy 1 Duchenne muscular dystrophy spinal muscular atrophy lateral sclerosis muscular dystrophy