Salla Disease

About the Disease
Salla Disease, also known as sd, is related to mucolipidosis and free sialic acid storage disorders, and has symptoms including ataxia, athetosis and muscle spasticity. An important gene associated with Salla Disease is SLC17A5 (Solute Carrier Family 17 Member 5), and among its related pathways/superpathways is Senescence and autophagy in cancer. Affiliated tissues include brain, and related phenotypes are intellectual disability and spasticity

Common Targets
SLC17A5

Note: If you'd like to get a target analysis report for Salla Disease, 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 Salla Disease at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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