Cauda Equina Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A peripheral nervous system disease that involves an acute loss of function of the lumbar plexus, neurologic elements (nerve roots) of the spinal canal below the termination (conus) of the spinal cord. (Human Disease Ontology, DOID_11577)
External Link https://www.disgenet.org/browser/0/1/0/C0392548
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Genes

3 genes associated with the disease Cauda Equina Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
HLA-B major histocompatibility complex, class I, B
LAMC2 laminin, gamma 2