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: C0234985
Disease: Mental deterioration
Mental deterioration
9 0 9 0.64 0 0
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
9 0 9 0.64 0 0
CUI: C0497327
Disease: Dementia
Dementia
17 12 4 0.15 2 1.5E-02
CUI: C0751587
Disease: CADASIL Syndrome
CADASIL Syndrome
2 0 2 0.14 0 0
CUI: C1449626
Disease: CADASILM
CADASILM
2 0 2 0.14 0 0
CUI: C2733158
Disease: Cerebral Small Vessel Diseases
Cerebral Small Vessel Diseases
5 1 2 0.12 1 8.0E-03
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
11 0 2 8.7E-02 0 0
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
13 0 2 8.0E-02 0 0
Childhood Ataxia with Central Nervous System Hypomyelinization
14 0 2 7.7E-02 0 0
CUI: C0038441
Disease: Stress Disorders, Traumatic
Stress Disorders, Traumatic
1 0 1 7.1E-02 0 0
CUI: C0039070
Disease: Syncope
Syncope
1 0 1 7.1E-02 0 0
CUI: C0344487
Disease: Lateral meningocele
Lateral meningocele
1 0 1 7.1E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia
1 0 1 7.1E-02 0 0
CUI: C1280768
Disease: Axenfeld syndrome
Axenfeld syndrome
1 0 1 7.1E-02 0 0
CUI: C1832916
Disease: Timothy syndrome
Timothy syndrome
1 0 1 7.1E-02 0 0
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
1 10 1 7.1E-02 1 7.5E-03
BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
1 0 1 7.1E-02 0 0
CUI: C1851710
Disease: LATERAL MENINGOCELE SYNDROME
LATERAL MENINGOCELE SYNDROME
1 0 1 7.1E-02 0 0
Macular Degeneration, Age-Related, 7
1 0 1 7.1E-02 0 0
CUI: C1860475
Disease: Retinal vascular tortuosity
Retinal vascular tortuosity
1 0 1 7.1E-02 0 0
CUI: C1867327
Disease: RETINAL ARTERIES, TORTUOSITY OF
RETINAL ARTERIES, TORTUOSITY OF
1 0 1 7.1E-02 0 0
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
1 0 1 7.1E-02 0 0
Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
1 0 1 7.1E-02 0 0
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3
1 0 1 7.1E-02 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
1 0 1 7.1E-02 0 0