[{"n": "Neuromuscular disease", "u": "/e/myoneural-junction-and-neuromuscular-diseases/neuromuscular-disease/", "s": "Disorders of the motor unit causing muscle weakness and atrophy."}, {"n": "Neuromuscular junction disease", "u": "/e/myoneural-junction-and-neuromuscular-diseases/neuromuscular-junction-disease/", "s": "Disorders of the motor end plate causing muscle weakness."}, {"n": "Acquired non-inflammatory myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/acquired-non-inflammatory-myopathy/", "s": "A non-autoimmune myopathy from drugs, metabolic issues, or nutritional deficits."}, {"n": "Central core disease", "u": "/e/myoneural-junction-and-neuromuscular-diseases/central-core-disease/", "s": "Autosomal dominant muscle disorder with risk of malignant hyperthermia."}, {"n": "Centronuclear myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/centronuclear-myopathy/", "s": "Congenital myopathy with centrally placed nuclei in muscle fibers."}, {"n": "Congenital myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/congenital-myopathy/", "s": "Genetic muscle disorders present at birth causing weakness."}, {"n": "Hyperkalemic periodic paralysis", "u": "/e/myoneural-junction-and-neuromuscular-diseases/hyperkalemic-periodic-paralysis/", "s": "Inherited disorder causing episodic muscle weakness and paralysis."}, {"n": "Hypokalemic periodic paralysis", "u": "/e/myoneural-junction-and-neuromuscular-diseases/hypokalemic-periodic-paralysis/", "s": "A channelopathy causing paralysis when potassium levels drop."}, {"n": "King-Denborough syndrome", "u": "/e/myoneural-junction-and-neuromuscular-diseases/king-denborough-syndrome/", "s": "A congenital myopathy with malignant hyperthermia susceptibility."}, {"n": "Lambert–Eaton myasthenic syndrome", "u": "/e/myoneural-junction-and-neuromuscular-diseases/lambert-eaton-myasthenic-syndrome/", "s": "An autoimmune disorder of neuromuscular transmission often linked to cancer."}, {"n": "Myotonia congenita", "u": "/e/myoneural-junction-and-neuromuscular-diseases/myotonia-congenita/", "s": "A genetic disorder causing delayed muscle relaxation after contraction."}, {"n": "Nemaline myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/nemaline-myopathy/", "s": "A congenital neuromuscular disorder with thread-like rods in muscle fibers."}, {"n": "Neuromyotonia", "u": "/e/myoneural-junction-and-neuromuscular-diseases/neuromyotonia/", "s": "A peripheral nerve hyperexcitability disorder causing spontaneous muscle activity."}, {"n": "Paramyotonia congenita", "u": "/e/myoneural-junction-and-neuromuscular-diseases/paramyotonia-congenita/", "s": "A rare disorder where cold and exercise worsen muscle stiffness."}, {"n": "Periodic paralysis", "u": "/e/myoneural-junction-and-neuromuscular-diseases/periodic-paralysis/", "s": "Rare genetic ion channel disorders causing episodic muscle weakness."}, {"n": "Sporadic late-onset nemaline myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/sporadic-late-onset-nemaline-myopathy/", "s": "A rare nemaline myopathy beginning after age 40."}, {"n": "Thyrotoxic myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/thyrotoxic-myopathy/", "s": "A neuromuscular disorder caused by excess thyroxine from hyperthyroidism."}, {"n": "Transient neonatal myasthenia gravis", "u": "/e/myoneural-junction-and-neuromuscular-diseases/transient-neonatal-myasthenia-gravis/", "s": "Temporary autoimmune muscle weakness in newborns of mothers with myasthenia gravis."}, {"n": "Ullrich congenital muscular dystrophy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/ullrich-congenital-muscular-dystrophy/", "s": "A congenital muscular dystrophy with contractures and joint laxity."}, {"n": "X-linked myotubular myopathy", "u": "/e/myoneural-junction-and-neuromuscular-diseases/x-linked-myotubular-myopathy/", "s": "Severe X-linked congenital muscle disease in male infants."}]