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Metadata
ID	SYMP:0000094
Name	muscle weakness
Parent Relationships	is_a muscle symptom
Related Diseases	has symptom infant botulism meningovascular neurosyphilis adult spinal muscular atrophy intermediate spinal muscular atrophy congenital muscular dystrophy Ullrich congenital muscular dystrophy Fukuyama congenital muscular dystrophy glycogen storage disease XV muscular dystrophy-dystroglycanopathy type B1 myotonic dystrophy type 2 X-linked myopathy with excessive autophagy Koolen de Vries syndrome inclusion body myopathy with Paget disease of bone and frontotemporal dementia Troyer syndrome hereditary hypophosphatemic rickets with hypercalciuria episodic ataxia type 7 episodic ataxia type 8 intrinsic cardiomyopathy familial hemiplegic migraine Native American myopathy hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 7 Miyoshi muscular dystrophy Miyoshi muscular dystrophy 2 spinal muscular atrophy with lower extremity predominant spinal muscular atrophy with lower extremity predominant 2A stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Compton-North congenital myopathy cylindrical spirals myopathy mitochondrial DNA depletion syndrome 2 mitochondrial DNA depletion syndrome 4b mitochondrial DNA depletion syndrome 11 multiple mitochondrial dysfunctions syndrome 1 Marinesco-Sjogren syndrome congenital muscular dystrophy with cataracts and intellectual disability myofibrillar myopathy myofibrillar myopathy 8 mitochondrial DNA depletion syndrome 12b congenital disorder of glycosylation It GNE myopathy congenital myopathy 6 Ehlers-Danlos syndrome musculocontractural type 2 polymyositis autosomal recessive limb-girdle muscular dystrophy type 2Z Brown-Vialetto-Van Laere syndrome 2 giant axonal neuropathy 2 rigid spine muscular dystrophy 1 congenital muscular dystrophy 1B congenital merosin-deficient muscular dystrophy 1A congenital myasthenic syndrome 8 congenital myasthenic syndrome 15 congenital myasthenic syndrome 12 congenital myasthenic syndrome 1B congenital myasthenic syndrome 1A congenital myasthenic syndrome 3C congenital myasthenic syndrome 3B congenital myasthenic syndrome 3A congenital myasthenic syndrome 14 congenital myasthenic syndrome 9 congenital myasthenic syndrome 19 congenital myasthenic syndrome 13 congenital myasthenic syndrome 4B congenital myasthenic syndrome 4A congenital myasthenic syndrome 4C congenital myasthenic syndrome 2C congenital myasthenic syndrome 2A congenital myasthenic syndrome 18 hereditary spastic paraplegia 3A hereditary spastic paraplegia 4 hereditary spastic paraplegia 5A nemaline myopathy 1 nemaline myopathy 9 nemaline myopathy 10 nemaline myopathy 11 nemaline myopathy 6 glycogen storage disease IXd autosomal recessive distal hereditary motor neuronopathy 2 myofibrillar myopathy 9 autosomal dominant adult-onset proximal spinal muscular atrophy X-linked distal spinal muscular atrophy 3 autosomal dominant distal hereditary motor neuronopathy 7 autosomal dominant distal hereditary motor neuronopathy 1 autosomal dominant distal hereditary motor neuronopathy 5 autosomal dominant distal hereditary motor neuronopathy 2 autosomal recessive distal hereditary motor neuronopathy 3 autosomal dominant distal hereditary motor neuronopathy 9 autosomal recessive distal hereditary motor neuronopathy 4 autosomal recessive distal hereditary motor neuronopathy 5 autosomal dominant distal hereditary motor neuronopathy 8 centronuclear myopathy 1 congenital muscular dystrophy-dystroglycanopathy type A NARP syndrome early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome myopathy with extrapyramidal signs autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 paramyotonia congenita of Von Eulenburg neurogenic scapuloperoneal syndrome Kaeser type scapuloperoneal spinal muscular atrophy Charcot-Marie-Tooth disease type 1G neurofibromatosis-Noonan syndrome nuclear type mitochondrial complex I deficiency 20 dermatomyositis distal myopathy myotonic dystrophy type 1 Duchenne muscular dystrophy juvenile spinal muscular atrophy spinal muscular atrophy Werdnig-Hoffmann disease Moebius syndrome myotonia congenita lateral sclerosis West Nile encephalitis nemaline myopathy HTLV-1-associated myelopathy/tropical spastic paraparesis inclusion body myositis congenital myasthenic syndrome myopathy Ebola virus disease myasthenia gravis myotonic disease postpoliomyelitis syndrome Becker muscular dystrophy muscular dystrophy peripartum cardiomyopathy