|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Incoordination of movement caused by a deficit in the sensory nervous system. Sensory ataxia can be distinguished from cerebellar ataxia by asking the patient to close his or her eyes. Persons with cerebellar ataxia show only a minimal worsening of symptoms, whereas persons with sensory ataxia show a marked worsening of symptoms. (Human Phenotype Ontology, HP_0010871)|
|Downloads & Tools|
7 genes associated with the sensory ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.