வார்ப்புரு:Diseases of myoneural junction and muscle
{{navbox | listclass = hlist
 | name  = Diseases of myoneural junction and muscle
 | title = Diseases of [[myoneural junction]] and [[muscle]] / [[neuromuscular disease]] ([[ICD-10_Chapter_G#.28G70-G73.29_Diseases_of_myoneural_junction_and_muscle|G70-G73]], [[List_of_ICD-9_codes_320-359:_Diseases_of_the_nervous_system#disorders_of_the_peripheral_nervous_system_.28350-359.29|358-359]]) 
 | state = {{{state|autocollapse}}}
 | titlestyle = background: Silver;
 | groupstyle = background-color: Linen; padding-left: 0.5em; padding-right: 0.75em
 | belowstyle = background:Linen
 
   | group1 = [[Neuromuscular junction disease|Neuromuscular-]]&lt;br /&gt;[[Neuromuscular junction disease|junction disease]]
   |  list1 = ''[[autoimmune]]'' ([[Myasthenia gravis]], [[Lambert–Eaton myasthenic syndrome]])
 
 | group3 = [[Myopathy]]/&lt;BR&gt;[[congenital myopathy]]
 |  list3 = {{navbox subgroup
   | groupstyle = background-color: Linen
   | evenodd = swap
 
 
   | group2 = [[Muscular dystrophy]]&lt;BR&gt;([[Dystrophin-associated protein complex|DAPC]])
   |  list2 = {{navbox subgroup
   | groupstyle = background-color: Linen
 
 | group1 = [[autosomal dominant|AD]]
 | list1  = [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 1]]{{·}} [[Oculopharyngeal muscular dystrophy|Oculopharyngeal]]{{·}} [[Facioscapulohumeral muscular dystrophy|Facioscapulohumeral]]{{·}} [[Myotonic dystrophy|Myotonic]]{{·}} [[Distal muscular dystrophy|Distal (most)]]
 
 | group2 = [[autosomal recessive|AR]]
 | list2  = [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 2]]{{·}} [[Congenital muscular dystrophy|Congenital]] ([[Fukuyama congenital muscular dystrophy|Fukuyama]], [[Ullrich congenital muscular dystrophy|Ullrich]])
 
 
 |group3  = [[X-linked recessive|XR]]
 |list3   = ''[[dystrophin]]'' ([[Becker's muscular dystrophy|Becker's]], [[Duchenne muscular dystrophy|Duchenne]]){{·}} [[Emery-Dreifuss muscular dystrophy|Emerin Emery-Dreifuss]]
 
 
 }}
 
 
   | group3 = Other structural
   |  list3 = ''[[collagen disease]]'' ([[Bethlem myopathy]]){{·}}  ''[[Protein tyrosine phosphatase|PTP disease]]'' ([[X-linked myotubular myopathy|X-linked MTM]]){{·}} ''[[adaptor protein|adaptor protein disease]]'' ([[Centronuclear myopathy|BIN1-linked centronuclear myopathy]]){{·}} ''[[cytoskeleton|cytoskeleton disease]]'' ([[Nemaline myopathy]], [[Zaspopathy]])
 
 
   | group4 = [[Channelopathy]]
   | list4  = {{navbox subgroup
   | groupstyle = background-color: Linen
 
 | group1 = [[Myotonia]]
 | list1  = [[Myotonia congenita]]{{·}} [[Thomsen disease]]{{·}} [[Neuromyotonia]]/[[Isaacs syndrome]]{{·}} [[Paramyotonia congenita]]
 
 | group2 = [[Periodic paralysis]]
 | list2  = [[Hypokalemic periodic paralysis|Hypokalemic]]{{·}} [[Hyperkalemic periodic paralysis|Hyperkalemic]]
 
 | group3 = Other
 | list3  = [[Central core disease]]
 
 
 }} 
 
   | group5 = [[Mitochondrial myopathy]]
   | list5  = [[Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes|MELAS]]{{·}} [[MERRF syndrome|MERRF]]{{·}} [[Kearns-Sayre syndrome|KSS]]{{·}} [[Progressive external ophthalmoplegia|PEO]] 
 
 
   | group7 = Other
   |  list7 = [[Inflammatory myopathy]]
 
 
 }}
 
 |  below = {{Muscle navs}}
 
 
 }}&lt;noinclude&gt;
 
 [[Category:Disease and disorder templates|{{PAGENAME}}]]