association	dataset	threshold value	standardized value
Decreased Vibratory Sense	DisGeNET Gene-Phenotype Associations	1.0	null
discovery	GeneRIF Biological Term Annotations	1.0	null
Hyperreflexia	DisGeNET Gene-Phenotype Associations	1.0	null
dysphagia	HPO Gene-Disease Associations	1.0	null
nystagmus	HPO Gene-Disease Associations	1.0	null
Parkinson Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
repeat	GeneRIF Biological Term Annotations	1.0	null
abnormal muscle tone	HPO Gene-Disease Associations	1.0	null
fluorescent	GeneRIF Biological Term Annotations	1.0	null
transcripts	GeneRIF Biological Term Annotations	1.0	null
type	GeneRIF Biological Term Annotations	1.0	null
slow saccadic eye movements	HPO Gene-Disease Associations	1.0	null
abnormality of nervous system morphology	HPO Gene-Disease Associations	1.0	null
Progressive Cerebellar Ataxia	DisGeNET Gene-Disease Associations	1.0	null
Cerebellar Atrophy	DisGeNET Gene-Disease Associations	1.0	null
abnormality of hindbrain morphology	HPO Gene-Disease Associations	1.0	null
parkinsons	GeneRIF Biological Term Annotations	1.0	null
greek	GeneRIF Biological Term Annotations	1.0	null
polyglutamine	GeneRIF Biological Term Annotations	1.0	null
Muscle Rigidity	DisGeNET Gene-Phenotype Associations	1.0	null
abnormality of the cerebellum	HPO Gene-Disease Associations	1.0	null
Dystonia	DisGeNET Gene-Phenotype Associations	1.0	null
autosomal dominant inheritance	HPO Gene-Disease Associations	1.0	null
Nystagmus	DisGeNET Gene-Disease Associations	1.0	null
Chronic Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
toxic	GeneRIF Biological Term Annotations	1.0	null
ataxia	HPO Gene-Disease Associations	1.0	null
peripheral neuropathy	HPO Gene-Disease Associations	1.0	null
Spasticity, Ctcae	DisGeNET Gene-Phenotype Associations	1.0	null
Pulmonary Aspiration	DisGeNET Gene-Phenotype Associations	1.0	null
sca8	GeneRIF Biological Term Annotations	1.0	null
abnormality of saccadic eye movements	HPO Gene-Disease Associations	1.0	null
cerebellar atrophy	HPO Gene-Disease Associations	1.0	null
suggests	GeneRIF Biological Term Annotations	1.0	null
Central Neuroblastoma	DisGeNET Gene-Disease Associations	1.0	null
Aspiration, Ctcae	DisGeNET Gene-Phenotype Associations	1.0	null
dysarthria	HPO Gene-Disease Associations	1.0	null
atxn8	GeneRIF Biological Term Annotations	1.0	null
intranuclear	GeneRIF Biological Term Annotations	1.0	null
Spinocerebellar Ataxia	DisGeNET Gene-Disease Associations	1.0	null
Muscle Spasticity	DisGeNET Gene-Phenotype Associations	1.0	null
detection	GeneRIF Biological Term Annotations	1.0	null
Pyramidal Sign	DisGeNET Gene-Phenotype Associations	1.0	null
Unintentional Material Aspiration	DisGeNET Gene-Phenotype Associations	1.0	null
sensory neuropathy	HPO Gene-Disease Associations	1.0	null
Urinary Incontinence	DisGeNET Gene-Phenotype Associations	1.0	null
Dysmetric Saccades	DisGeNET Gene-Phenotype Associations	1.0	null
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias	GAD Gene-Disease Associations	1.0	null
incoordination	HPO Gene-Disease Associations	1.0	null
posttranscriptional	GeneRIF Biological Term Annotations	1.0	null
one	GeneRIF Biological Term Annotations	1.0	null
Ataxia	DisGeNET Gene-Phenotype Associations	1.0	null
Slowed Saccades	DisGeNET Gene-Phenotype Associations	1.0	null
Gait, Unsteady	DisGeNET Gene-Phenotype Associations	1.0	null
Morphological Abnormality Of The Pyramidal Tract	DisGeNET Gene-Disease Associations	1.0	null
morphological abnormality of the central nervous system	HPO Gene-Disease Associations	1.0	null
abnormality of the abdomen	HPO Gene-Disease Associations	1.0	null
opposite	GeneRIF Biological Term Annotations	1.0	null
cerebellar ataxia;	GAD Gene-Disease Associations	1.0	null
caused	GeneRIF Biological Term Annotations	1.0	null
dysmetric saccades	HPO Gene-Disease Associations	1.0	null
taiwanese	GeneRIF Biological Term Annotations	1.0	null
abnormality of central motor function	HPO Gene-Disease Associations	1.0	null
abnormality of ocular smooth pursuit	HPO Gene-Disease Associations	1.0	null
abnormal pyramidal signs	HPO Gene-Disease Associations	1.0	null
abnormality of the metencephalon	HPO Gene-Disease Associations	1.0	null
Dysarthria	DisGeNET Gene-Phenotype Associations	1.0	null
atxn8os	GeneRIF Biological Term Annotations	1.0	null
Cerebellar Ataxia	HuGE Navigator Gene-Phenotype Associations	1.0	null
Childhood Neuroblastoma	DisGeNET Gene-Disease Associations	1.0	null
morphological abnormality of the pyramidal tract	HPO Gene-Disease Associations	1.0	null
abnormality of higher mental function	HPO Gene-Disease Associations	1.0	null
inclusions	GeneRIF Biological Term Annotations	1.0	null
patient	GeneRIF Biological Term Annotations	1.0	null
all	HPO Gene-Disease Associations	1.0	null
Genetic Predisposition to Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
Facial Grimacing	DisGeNET Gene-Phenotype Associations	1.0	null
abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
pathogenesis	GeneRIF Biological Term Annotations	1.0	null
epigenetic	GeneRIF Biological Term Annotations	1.0	null
only	GeneRIF Biological Term Annotations	1.0	null
abnormal eye physiology	HPO Gene-Disease Associations	1.0	null
abnormality of brain morphology	HPO Gene-Disease Associations	1.0	null
expanded	GeneRIF Biological Term Annotations	1.0	null
repeats	GeneRIF Biological Term Annotations	1.0	null
neurological speech impairment	HPO Gene-Disease Associations	1.0	null
Endotracheal Aspiration	DisGeNET Gene-Phenotype Associations	1.0	null
trinucleotide	GeneRIF Biological Term Annotations	1.0	null
susceptibility	GeneRIF Biological Term Annotations	1.0	null
abnormal involuntary eye movements	HPO Gene-Disease Associations	1.0	null
Spinocerebellar ataxia 8	CTD Gene-Disease Associations	1.0	2.88009
strand	GeneRIF Biological Term Annotations	1.0	null
mechanisms	GeneRIF Biological Term Annotations	1.0	null
Bradykinesia	DisGeNET Gene-Phenotype Associations	1.0	null
morphological abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
mode of inheritance	HPO Gene-Disease Associations	1.0	null
abnormality of the abdominal organs	HPO Gene-Disease Associations	1.0	null
hypertonia	HPO Gene-Disease Associations	1.0	null
huntingtons	GeneRIF Biological Term Annotations	1.0	null
method	GeneRIF Biological Term Annotations	1.0	null
Postural Instability	DisGeNET Gene-Phenotype Associations	1.0	null
Tremor	DisGeNET Gene-Phenotype Associations	1.0	null
Parkinson Disease	DisGeNET Gene-Disease Associations	1.0	null
Nystagmus	DisGeNET Gene-Phenotype Associations	1.0	null
Impaired Smooth Pursuit	DisGeNET Gene-Phenotype Associations	1.0	null
Neuroblastoma	DisGeNET Gene-Disease Associations	1.0	null
Actual Aspiration	DisGeNET Gene-Phenotype Associations	1.0	null
ataxin	GeneRIF Biological Term Annotations	1.0	null
abnormal peripheral nervous system morphology	HPO Gene-Disease Associations	1.0	null
abnormality of the eye	HPO Gene-Disease Associations	1.0	null
abnormality of muscle physiology	HPO Gene-Disease Associations	1.0	null
Parkinsonian Disorders	HuGE Navigator Gene-Phenotype Associations	1.0	null
Hypoplasia	DisGeNET Gene-Phenotype Associations	1.0	null
abnormality of movement	HPO Gene-Disease Associations	1.0	null
Spinocerebellar Ataxias	HuGE Navigator Gene-Phenotype Associations	1.0	null
affects	GeneRIF Biological Term Annotations	1.0	null
polymorphism	GeneRIF Biological Term Annotations	1.0	null
phenotypic abnormality	HPO Gene-Disease Associations	1.0	null
abnormality of eye movement	HPO Gene-Disease Associations	1.0	null
upper motor neuron dysfunction	HPO Gene-Disease Associations	1.0	null
rna	GeneRIF Biological Term Annotations	1.0	null
involves	GeneRIF Biological Term Annotations	1.0	null
progressive cerebellar ataxia	HPO Gene-Disease Associations	1.0	null
spasticity	HPO Gene-Disease Associations	1.0	null
Abnormal Coordination	DisGeNET Gene-Phenotype Associations	1.0	null
report	GeneRIF Biological Term Annotations	1.0	null
Erectile Dysfunction	DisGeNET Gene-Disease Associations	1.0	null
Dysarthria	DisGeNET Gene-Disease Associations	1.0	null
stability	GeneRIF Biological Term Annotations	1.0	null
Gait Ataxia	DisGeNET Gene-Phenotype Associations	1.0	null
abnormality of the nervous system	HPO Gene-Disease Associations	1.0	null
expansion	GeneRIF Biological Term Annotations	1.0	null
tremor	HPO Gene-Disease Associations	1.0	null
Cerebellar Vermis Atrophy	DisGeNET Gene-Phenotype Associations	1.0	null
noncoding	GeneRIF Biological Term Annotations	1.0	null
ataxia	GeneRIF Biological Term Annotations	1.0	null
abnormality of nervous system physiology	HPO Gene-Disease Associations	1.0	null
Alzheimer Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of coordination	HPO Gene-Disease Associations	1.0	null
impaired smooth pursuit	HPO Gene-Disease Associations	1.0	null
gainoffunction	GeneRIF Biological Term Annotations	1.0	null
pcr	GeneRIF Biological Term Annotations	1.0	null
abnormality of the musculature	HPO Gene-Disease Associations	1.0	null
abnormality of the esophagus	HPO Gene-Disease Associations	1.0	null
Central Nervous System Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
spinocerebellar	GeneRIF Biological Term Annotations	1.0	null
spinocerebellar ataxia 8	OMIM Gene-Disease Associations	1.0	null
Depression	DisGeNET Gene-Disease Associations	1.0	null
Atypical Parkinsonism	DisGeNET Gene-Disease Associations	1.0	null