vertical supranuclear gaze palsy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A supranuclear gaze palsy is an inability to look in a vertical direction as a result of cerebral impairment. There is a loss of the voluntary aspect of eye movements, but, as the brainstem is still intact, all the reflex conjugate eye movements are normal. (Human Phenotype Ontology, HP_0000511)
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3 genes associated with the vertical supranuclear gaze palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DCTN1 dynactin 1
NPC1 Niemann-Pick disease, type C1
NPC2 Niemann-Pick disease, type C2