degeneration of the lateral corticospinal tracts Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Deterioration of the tissues of the lateral corticospinal tracts. (Human Phenotype Ontology, HP_0002314)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002314
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Genes

8 genes associated with the degeneration of the lateral corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL1 atlastin GTPase 1
KIAA0196 KIAA0196
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)