Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3554690
Disease: ATAXIA-OCULOMOTOR APRAXIA 3
ATAXIA-OCULOMOTOR APRAXIA 3
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3554690
Disease: ATAXIA-OCULOMOTOR APRAXIA 3
ATAXIA-OCULOMOTOR APRAXIA 3
0.700 GeneticVariation disease UNIPROT A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia. 22065524 2012
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.300 GeneticVariation disease UNIPROT
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1
0.300 GermlineCausalMutation disease ORPHANET A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia. 22065524 2012
CUI: C0004134
Disease: Ataxia
Ataxia
0.110 Biomarker phenotype HPO
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome
0.110 Biomarker disease HPO
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia
0.110 Biomarker disease HPO
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.100 Biomarker group HPO
CUI: C0013362
Disease: Dysarthria
Dysarthria
0.100 Biomarker disease HPO
CUI: C0013421
Disease: Dystonia
Dystonia
0.100 Biomarker phenotype HPO
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.100 Biomarker disease HPO
CUI: C0020580
Disease: Hypesthesia
Hypesthesia
0.100 Biomarker phenotype HPO
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.100 Biomarker disease HPO
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
0.100 Biomarker phenotype HPO
CUI: C0038379
Disease: Strabismus
Strabismus
0.100 Biomarker disease HPO
CUI: C0085583
Disease: Choreoathetosis
Choreoathetosis
0.100 Biomarker disease HPO
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
0.100 Biomarker phenotype HPO
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
0.100 Biomarker phenotype HPO
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy
0.100 Biomarker disease HPO
CUI: C0234146
Disease: Absent reflex
Absent reflex
0.100 Biomarker phenotype HPO
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
0.100 Biomarker phenotype HPO
CUI: C0234378
Disease: Static Tremor
Static Tremor
0.100 Biomarker phenotype HPO
CUI: C0235971
Disease: Elevated alpha-fetoprotein
Elevated alpha-fetoprotein
0.100 Biomarker phenotype HPO
CUI: C0239882
Disease: Head tremor
Head tremor
0.100 Biomarker phenotype HPO
CUI: C0239981
Disease: Hypoalbuminemia
Hypoalbuminemia
0.100 Biomarker disease HPO