abnormality of the corticospinal tract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the corticospinal tract, which is the chief element of the pyramidal system (the principle motor tract) and is the only direct connection between the cerebrum and the spinal cord. (Human Phenotype Ontology, HP_0002492)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002492
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10 genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
ATL1 atlastin GTPase 1
KIAA0196 KIAA0196
L1CAM L1 cell adhesion molecule
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
PLP1 proteolipid protein 1
SOD1 superoxide dismutase 1, soluble
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)