Paraplegia

About the Disease
Paraplegia, also known as severe or complete loss of motor function in the lower extremities and lower portions of the trunk, is related to spastic paraplegia 5a, autosomal recessive and spastic paraplegia 6, autosomal dominant, and has symptoms including hemiplegia, ophthalmoplegia and paraparesis. An important gene associated with Paraplegia is SLC33A1 (Solute Carrier Family 33 Member 1). The drugs Acetylcholine and Cholinergic Agents have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and bone marrow, and related phenotypes are no effect and no effect

Common Targets
RARB

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