Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751495
Disease: Seizures, Focal
Seizures, Focal
0.160 Biomarker phenotype HPO
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus
0.150 Biomarker disease HPO
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures
0.150 Biomarker disease HPO
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
0.140 Biomarker disease HPO
CUI: C0004134
Disease: Ataxia
Ataxia
0.130 Biomarker phenotype HPO
CUI: C0456909
Disease: Blindness
Blindness
0.120 Biomarker phenotype HPO
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.110 CausalMutation disease CLINVAR
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
0.110 Biomarker phenotype HPO
CUI: C0018991
Disease: Hemiplegia
Hemiplegia
0.110 Biomarker phenotype HPO
CUI: C0027066
Disease: Myoclonus
Myoclonus
0.110 Biomarker phenotype HPO
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.110 Biomarker phenotype HPO
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.110 GeneticVariation phenotype CLINVAR
CUI: C0270846
Disease: Epileptic drop attack
Epileptic drop attack
0.110 Biomarker disease HPO
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
0.110 Biomarker phenotype HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.110 Biomarker disease HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.110 CausalMutation disease CLINVAR
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
0.110 Biomarker disease HPO
Malformations of Cortical Development, Group II
0.110 CausalMutation disease CLINVAR
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
0.110 Biomarker phenotype HPO
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
0.100 Biomarker phenotype HPO
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
0.100 Biomarker phenotype HPO
CUI: C0003467
Disease: Anxiety
Anxiety
0.100 Biomarker disease HPO
CUI: C0011071
Disease: Sudden death
Sudden death
0.100 CausalMutation phenotype CLINVAR
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.100 Biomarker phenotype HPO
CUI: C0017639
Disease: Gliosis
Gliosis
0.100 CausalMutation phenotype CLINVAR