Amyotrophic Lateral Sclerosis 1 (ALS1)

Amyotrophic Lateral Sclerosis 1(来自ICD-11)

别称:

Amyotrophic Lateral Sclerosis

Als

Lou Gehrig Disease

Charcot Disease

Amyotrophic Lateral Sclerosis Type 1

Amyotrophic Lateral Sclerosis, Susceptibility to

Als1

Familial Amyotrophic Lateral Sclerosis

Motor Neuron Disease

Lou Gehrig's Disease

Fals

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis with Dementia

Dementia with Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Sclerosis, Lateral, Amyotrophic, Type 1

Als - [amyotrophic Lateral Sclerosis]

Sclerosis, Lateral, Amyotrophic

Progressive Atrophic Paralysis

Spinal Progressive Amyotrophy

Motor Neuron Disease, Bulbar

Amyotrophy Lateral Sclerosis

Amyotrophic Sclerosis

Amyotrophic Paralysis

Wasting Paralysis

Wasting Palsy

Mnd

加入收藏

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Amyotrophic Lateral Sclerosis 1, also known as amyotrophic lateral sclerosis, is related to frontotemporal dementia and/or amyotrophic lateral sclerosis 1 and frontotemporal dementia, and has symptoms including back pain, headache and pain. An important gene associated with Amyotrophic Lateral Sclerosis 1 is SOD1 (Superoxide Dismutase 1), and among its related pathways/superpathways are Neuroscience and Physico-chemical features and toxicity-associated pathways. The drugs Mexiletine and Cannabidiol have been mentioned in the context of this disorder. Affiliated tissues include Bone, Limb and spinal cord, and related phenotypes are amyotrophic lateral sclerosis and generalized muscle weakness

查看原文参与反馈