sensory ataxia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010871
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Genes

7 genes associated with the sensory ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
EGR2 early growth response 2
FLVCR1 feline leukemia virus subgroup C cellular receptor 1
GPI glucose-6-phosphate isomerase
MPZ myelin protein zero
PMP22 peripheral myelin protein 22
PRX periaxin