Paraplegia

Alias:
Paraplegia, Lower
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Paraplegia, also known as paraplegia, lower, is related to spastic paraplegia 48, autosomal recessive and spastic paraplegia 15, autosomal recessive, 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 Dronabinol have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and brain, and related phenotypes are nervous system and growth/size/body region
Related ID:
MESH:D010264

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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56
308
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Medical Symptom

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Description
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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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