cervical cord compression Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Compression of the spinal cord in the cervical region, generally manifested by paresthesias and numbness, weakness, difficulty walking, abnormalities of coordination, and neck pain or stiffness. (Human Phenotype Ontology, HP_0002341)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002341
Similar Terms
Downloads & Tools

Genes

3 genes associated with the cervical cord compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COMP cartilage oligomeric matrix protein
IDS iduronate 2-sulfatase
RMRP RNA component of mitochondrial RNA processing endoribonuclease