: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
| list1 =
- autoimmune
- Myasthenia gravis
- Lambert–Eaton myasthenic syndrome
- Neuromyotonia
- Congenital myasthenic syndrome
| group3 = Myopathy
| list3 =
{{Navbox|subgroup
| evenodd = swap
| group2 = Muscular dystrophy
(DAPC)
| list2 =
{{Navbox|subgroup
| group1 = AD
| list1 =
| group2 = AR
| list2 =
| group3 = XR
| list3 =
}}
| group3 = Other structural
| list3 =
- collagen disease
- Bethlem myopathy
- PTP disease
- X-linked MTM
- adaptor protein disease
- BIN1-linked centronuclear myopathy
- 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 =
| group3 = Other
| list3 =
}}
| group5 = ATPase disorder
- (ion pump)
| list5 =
| group6 = Metabolic myopathy
| list6 =
- Muscle Glycogen storage disease
- Fatty-acid metabolism disorder
- AMPD1 deficiency
- Mitochondrial myopathy (MELAS
- MERRF
- KSS
- PEO
- MNGIE)
| group7 = Endocrinopathy
| list7 =
- Hypothyroid myopathy
- Kocher–Debre–Semelaigne syndrome
- Hoffmann syndrome
- Hyperthyroid myopathy
- Thyrotoxic myopathy
- Hypoparathyroid myopathy
- Hyperparathyroid myopathy
- Hypercortisolism
- Corticosteroid myopathy
- Testosterone deficiency myopathy
- Late-onset hypogonadism
- Hypogonadotropic hypogonadism
- Androgen deficiency
| group8 = General
| list8 =
}}
}}
{{collapsible option}}