Amyotrophic Lateral Sclerosis Type 6 (ALS6)

Alias:
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
Amyotrophic Lateral Sclerosis 6, with or Without Frontotemporal Dementia
Autosomal Recessive Amyotrophic Lateral Sclerosis 6
Amyotrophic Lateral Sclerosis 6
Als6
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Amyotrophic Lateral Sclerosis Type 6, also known as amyotrophic lateral sclerosis 6, autosomal recessive, is related to amyotrophic lateral sclerosis 6 with or without frontotemporal dementia and frontotemporal dementia and/or amyotrophic lateral sclerosis 6. An important gene associated with Amyotrophic Lateral Sclerosis Type 6 is FUS (FUS RNA Binding Protein), and among its related pathways/superpathways is Neuroscience. Affiliated tissues include endothelial and brain, and related phenotypes are nervous system and homeostasis/metabolism
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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24
213
55

Medical Symptom

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Description
HPO Frequency
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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