Faster access than browser!Similarities between Atrophy and ICD-10 Chapter VI: Diseases of the nervous system
Atrophy and ICD-10 Chapter VI: Diseases of the nervous system have 7 things in common (in Unionpedia): Amyotrophic lateral sclerosis, Charcot–Marie–Tooth disease, Guillain–Barré syndrome, Muscular dystrophy, Myotonia congenita, Myotonic dystrophy, Spinal muscular atrophies.
Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND), and Lou Gehrig's disease, is a specific disease which causes the death of neurons controlling voluntary muscles.
Amyotrophic lateral sclerosis and Atrophy · Amyotrophic lateral sclerosis and ICD-10 Chapter VI: Diseases of the nervous system ·
Charcot–Marie–Tooth disease
Charcot–Marie–Tooth disease (CMT) is one of the hereditary motor and sensory neuropathies, a group of varied inherited disorders of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body.
Atrophy and Charcot–Marie–Tooth disease · Charcot–Marie–Tooth disease and ICD-10 Chapter VI: Diseases of the nervous system ·
Guillain–Barré syndrome
Guillain–Barré syndrome (GBS) is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system.
Atrophy and Guillain–Barré syndrome · Guillain–Barré syndrome and ICD-10 Chapter VI: Diseases of the nervous system ·
Muscular dystrophy
Muscular dystrophy (MD) is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time.
Atrophy and Muscular dystrophy · ICD-10 Chapter VI: Diseases of the nervous system and Muscular dystrophy ·
Myotonia congenita
Congenital myotonia, also called myotonia congenita, is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement).
Atrophy and Myotonia congenita · ICD-10 Chapter VI: Diseases of the nervous system and Myotonia congenita ·
Myotonic dystrophy
Myotonic dystrophy is a long term genetic disorder that affects muscle function.
Atrophy and Myotonic dystrophy · ICD-10 Chapter VI: Diseases of the nervous system and Myotonic dystrophy ·
Spinal muscular atrophies
Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body.
Atrophy and Spinal muscular atrophies · ICD-10 Chapter VI: Diseases of the nervous system and Spinal muscular atrophies ·
The list above answers the following questions
- What Atrophy and ICD-10 Chapter VI: Diseases of the nervous system have in common
- What are the similarities between Atrophy and ICD-10 Chapter VI: Diseases of the nervous system
Atrophy and ICD-10 Chapter VI: Diseases of the nervous system Comparison
Atrophy has 45 relations, while ICD-10 Chapter VI: Diseases of the nervous system has 259. As they have in common 7, the Jaccard index is 2.30% = 7 / (45 + 259).
References
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