Category:Myoneural junction and neuromuscular diseases

This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes G70-G73 should be included in this category.

Subcategories

This category has the following 2 subcategories, out of 2 total.

M

• ► Motor neuron diseases‎ (1 C, 23 P)
• ► Muscular dystrophy‎ (1 C, 70 P)

Pages in category "Myoneural junction and neuromuscular diseases"

The following 27 pages are in this category, out of 27 total.

B

• Bethlem myopathy
• Botulism

C

• Central core disease
• Autosomal dominant centronuclear myopathy
• Autosomal recessive centronuclear myopathy
• Centronuclear myopathy
• Congenital myasthenic syndromes
• Tubular aggregate myopathy

F

• Familial periodic paralyses
• Fields' disease

I

• Intermediate congenital nemaline myopathy
• Isaacs' syndrome

L

• Lambert Eaton myasthenic syndrome
• Late-onset distal myopathy, Markesbery-Griggs type

M

• Myasthenia - congenital
• Myasthenia gravis
• Myoclonic epilepsy with ragged red fibers
• Becker's myotonia
• Myotonic dystrophy
• Myotonic dystrophy type 1
• Myotonic dystrophy type 2

N

• Nemaline myopathy
• Neuromyotonia

P

• Periodic paralysis

T

• Thyrotoxic myopathy

U

• Ullrich congenital muscular dystrophy

X

• X-linked myotubular myopathy

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Categories:

• Neurological disorders by disease category
• Musculoskeletal disorders