Source: CURATED ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0014549
Disease: Tonic-Clonic Epilepsy
Tonic-Clonic Epilepsy 		10 0 2 1.0E-01 0 0
CUI: C0751117
Disease: Cryptogenic Tonic-Clonic Epilepsy
Cryptogenic Tonic-Clonic Epilepsy 		10 0 2 1.0E-01 0 0
CUI: C0751118
Disease: Epilepsy, Tonic-Clonic, Familial
Epilepsy, Tonic-Clonic, Familial 		10 0 2 1.0E-01 0 0
CUI: C0751119
Disease: Epilepsy, Tonic-Clonic, Symptomatic
Epilepsy, Tonic-Clonic, Symptomatic 		10 0 2 1.0E-01 0 0
CUI: C0028797
Disease: Occupational Diseases
Occupational Diseases 		11 0 2 9.5E-02 0 0
CUI: C0393574
Disease: Huntington Disease, Late Onset
Huntington Disease, Late Onset 		12 0 2 9.1E-02 0 0
CUI: C0751207
Disease: Akinetic-Rigid Variant of Huntington Disease
Akinetic-Rigid Variant of Huntington Disease 		12 0 2 9.1E-02 0 0
CUI: C0751208
Disease: Juvenile Huntington Disease
Juvenile Huntington Disease 		12 0 2 9.1E-02 0 0
CUI: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases 		1 0 1 8.3E-02 0 0
CUI: C0003431
Disease: Antisocial Personality Disorder
Antisocial Personality Disorder 		1 0 1 8.3E-02 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		1 0 1 8.3E-02 0 0
CUI: C0013409
Disease: Dyssocial Behavior
Dyssocial Behavior 		1 0 1 8.3E-02 0 0
CUI: C0019112
Disease: Hemorrhoids
Hemorrhoids 		1 0 1 8.3E-02 0 0
CUI: C0031030
Disease: Periapical Periodontitis
Periapical Periodontitis 		1 0 1 8.3E-02 0 0
CUI: C0158850
Disease: Fetal Malnutrition
Fetal Malnutrition 		1 0 1 8.3E-02 0 0
CUI: C0282550
Disease: Persian Gulf Syndrome
Persian Gulf Syndrome 		1 0 1 8.3E-02 0 0
CUI: C0524686
Disease: Periodontitis, Acute Nonsuppurative
Periodontitis, Acute Nonsuppurative 		1 0 1 8.3E-02 0 0
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome 		1 0 1 8.3E-02 0 0
CUI: C1285261
Disease: Fetal Nutrition Disorders
Fetal Nutrition Disorders 		1 0 1 8.3E-02 0 0
CUI: C1837154
Disease: Drug Metabolism, Poor, CYP2D6-Related
Drug Metabolism, Poor, CYP2D6-Related 		1 0 1 8.3E-02 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 8.3E-02 0 0
CUI: C1848587
Disease: Isolated hypoplasia of the right ventricle
Isolated hypoplasia of the right ventricle 		1 0 1 8.3E-02 0 0
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
Ataxia-Telangiectasia Variant 		1 0 1 8.3E-02 0 0
CUI: C2674665
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding) 		1 0 1 8.3E-02 0 0
CUI: C3280587
Disease: AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE
AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE 		1 0 1 8.3E-02 0 0