Template: Diseases of myoneural junction and muscle

{{Navbox
| name       = Diseases of myoneural junction and muscle
| title      = Diseases of [[muscle]], [[neuromuscular junction]], and [[neuromuscular disease]]
| listclass  = hlist
| state      = {{{state|autocollapse}}}

| group1 = [[Neuromuscular junction disease|Neuromuscular-]]<br />[[Neuromuscular junction disease|junction disease]]
| list1  = 
* ''[[autoimmune]]''
** [[Myasthenia gravis]]
** [[Lambert–Eaton myasthenic syndrome]]
** [[Neuromyotonia]]
*  [[Congenital myasthenic syndrome]]
| group3  = [[Myopathy]]
| list3  =
  {{Navbox|subgroup
  
  | evenodd    = swap

  | group2  = [[Muscular dystrophy]]<br />([[Dystrophin-associated protein complex|DAPC]])
  | list2  =
    {{Navbox|subgroup

    | 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  = 
* [[Calpainopathy]]
* [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 2]]
* [[Congenital muscular dystrophy|Congenital]]
** [[Fukuyama congenital muscular dystrophy|Fukuyama]]
** [[Ullrich congenital muscular dystrophy|Ullrich]]
** [[Walker–Warburg syndrome|Walker–Warburg]]

    | group3 = [[X-linked recessive|XR]]
    | list3  = 
* ''[[dystrophin]]''
** [[Becker's muscular dystrophy|Becker's]]
** [[Duchenne muscular dystrophy|Duchenne]]
* [[Emery–Dreifuss muscular dystrophy|Emery–Dreifuss]]
  }}

| group3 = Other structural
| list3  = 
* ''[[collagen disease]]''
** [[Bethlem myopathy]]
* ''[[Protein tyrosine phosphatase|PTP disease]]''
** [[X-linked myotubular myopathy|X-linked MTM]]
* ''[[Signal transducing adaptor protein|adaptor protein disease]]''
** [[Centronuclear myopathy|BIN1-linked centronuclear myopathy]]
* ''[[cytoskeleton|cytoskeleton disease]]''
** [[Nemaline myopathy]]
** [[Zaspopathy]]

| group4  = [[Channelopathy]] 
*(ion channel)
| list4  = 
  {{Navbox|subgroup

  | group1 = [[Myotonia]]
  | list1  = 
* [[Myotonia congenita]]
** [[Thomsen disease]]
** [[Becker disease]]
* [[Neuromyotonia]]
**[[Isaacs syndrome]]
* [[Paramyotonia congenita]]

  | group2 = [[Periodic paralysis]]
  | list2  = 
* [[Hypokalemic periodic paralysis|Hypokalemic]]
** [[Thyrotoxic periodic paralysis|Thyrotoxic]]
* [[Hyperkalemic periodic paralysis|Hyperkalemic]]

  | group3 = Other
  | list3  = 
* [[Central core disease]]
  }}

| group5 = ATPase disorder
* (ion pump)
| list5  = 
* [[Brody myopathy|Brody disease]] ([[ATP2A1]])

| group6 = [[Metabolic myopathy]]
| list6  = 
* Muscle [[Glycogen storage disease]]
* [[Fatty-acid metabolism disorder]]
* [[Adenosine monophosphate deaminase deficiency type 1|AMPD1 deficiency]]
* [[Mitochondrial myopathy]] ([[MELAS syndrome|MELAS]]
* [[MERRF syndrome|MERRF]]
* [[Kearns–Sayre syndrome|KSS]]
* [[Chronic progressive external ophthalmoplegia|PEO]]
* [[Mitochondrial neurogastrointestinal encephalopathy syndrome|MNGIE]])

| group7 = [[Endocrine disease|Endocrinopathy]]
| list7  =
* [[Hypothyroid]] myopathy
** [[Kocher–Debre–Semelaigne syndrome]]
** [[Hoffmann syndrome]]
* [[Hyperthyroid]] myopathy 
** [[Thyrotoxic myopathy]]
* [[Hypoparathyroidism|Hypoparathyroid myopathy]] 
* [[Hyperparathyroidism|Hyperparathyroid myopathy]]
* [[Hypercortisolism]] 
** Corticosteroid myopathy
* Testosterone deficiency myopathy
** [[Late-onset hypogonadism]]
** [[Hypogonadotropic hypogonadism]]
** [[Androgen deficiency]]

| group8 = General
| list8  = 
* [[Inflammatory myopathy]]
* [[Congenital myopathy]]
}}

}}<noinclude>
{{collapsible option}}
[[Category:Myoneural junction and neuromuscular diseases]]
[[Category:Neurological disorders templates]]

</noinclude>