Distal Myopathy 2

About the Disease
Amyotrophic Lateral Sclerosis 21, also known as amyotrophic lateral sclerosis type 21, is related to multisystem proteinopathy and distal hereditary motor neuronopathy type 7, and has symptoms including upper motor neuron signs An important gene associated with Amyotrophic Lateral Sclerosis 21 is MATR3 (Matrin 3), and among its related pathways/superpathways is Amyotrophic lateral sclerosis (ALS). Affiliated tissues include spinal cord, skeletal muscle and cortex, and related phenotypes are hyperreflexia and dysarthria

Common Targets
MATR3 | KLHL9 | MYH14 | MYH7

Note: If you'd like to get a target analysis report for Distal Myopathy 2, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Distal Myopathy 2 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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