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: C0017677
Disease: Glossitis, Benign Migratory
Glossitis, Benign Migratory
53 0 14 6.6E-02 0 0
CUI: C0232197
Disease: Fibrillation
Fibrillation
118 0 18 6.6E-02 0 0
CUI: C3887551
Disease: Memory dysfunction
Memory dysfunction
70 0 15 6.6E-02 0 0
CUI: C0220756
Disease: Niemann-Pick Disease, Type C
Niemann-Pick Disease, Type C
201 0 23 6.5E-02 0 0
CUI: C0038358
Disease: Gastric ulcer
Gastric ulcer
136 0 19 6.5E-02 0 0
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
185 0 22 6.5E-02 0 0
CUI: C0917798
Disease: Cerebral Ischemia
Cerebral Ischemia
120 0 18 6.5E-02 0 0
CUI: C1565662
Disease: Acute Kidney Insufficiency
Acute Kidney Insufficiency
104 0 17 6.5E-02 0 0
CUI: C0026847
Disease: Spinal Muscular Atrophy
Spinal Muscular Atrophy
320 0 30 6.5E-02 0 0
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
108 0 17 6.4E-02 0 0
CUI: C0271680
Disease: Diabetic Polyneuropathies
Diabetic Polyneuropathies
42 0 13 6.4E-02 0 0
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack
344 0 31 6.4E-02 0 0
CUI: C1402315
Disease: Vascular lesions
Vascular lesions
111 0 17 6.3E-02 0 0
CUI: C0025261
Disease: Memory Disorders
Memory Disorders
62 0 14 6.3E-02 0 0
CUI: C0872084
Disease: Sarcopenia
Sarcopenia
164 0 20 6.3E-02 0 0
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
522 0 41 6.3E-02 0 0
CUI: C0007682
Disease: CNS disorder
CNS disorder
319 0 29 6.2E-02 0 0
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
219 0 23 6.2E-02 0 0
CUI: C0221505
Disease: Lesion of brain
Lesion of brain
188 0 21 6.2E-02 0 0
CUI: C0022336
Disease: Creutzfeldt-Jakob disease
Creutzfeldt-Jakob disease
137 52 18 6.1E-02 3 2.1E-02
Primary Progressive Aphasia (disorder)
51 11 13 6.1E-02 2 1.9E-02
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
260 0 25 6.1E-02 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
434 0 35 6.1E-02 0 0
CUI: C1562113
Disease: Fleck corneal dystrophy
Fleck corneal dystrophy
104 0 16 6.1E-02 0 0
Behavioral variant of frontotemporal dementia
35 10 12 6.1E-02 1 9.5E-03