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: C2900450
Disease: Other Creutzfeldt-Jakob disease
Other Creutzfeldt-Jakob disease
37 18 37 0.27 18 0.35
CUI: C1852467
Disease: Creutzfeldt-Jakob Disease, Sporadic
Creutzfeldt-Jakob Disease, Sporadic
57 23 39 0.25 13 0.21
CUI: C0162534
Disease: Prion Diseases
Prion Diseases
175 67 46 0.17 23 0.24
CUI: C4310512
Disease: Sporadic CJD
Sporadic CJD
30 17 23 0.16 15 0.28
New Variant Creutzfeldt-Jakob Disease
23 2 21 0.15 2 3.8E-02
CUI: C0751254
Disease: Creutzfeldt-Jakob Disease, Familial
Creutzfeldt-Jakob Disease, Familial
22 16 20 0.14 13 0.24
CUI: C0333463
Disease: Senile Plaques
Senile Plaques
249 21 37 0.11 1 1.4E-02
CUI: C0949664
Disease: Tauopathies
Tauopathies
245 0 36 0.10 0 0
CUI: C0265101
Disease: Carotid artery occlusion
Carotid artery occlusion
74 0 19 9.9E-02 0 0
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
212 32 31 9.7E-02 1 1.2E-02
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid
123 10 23 9.7E-02 1 1.6E-02
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia
25 16 14 9.5E-02 8 0.13
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain
213 83 30 9.4E-02 2 1.5E-02
CUI: C0025587
Disease: Metatarsalgia
Metatarsalgia
15 0 13 9.4E-02 0 0
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy
182 0 27 9.2E-02 0 0
CUI: C2242710
Disease: Intra-Abdominal Hypertension
Intra-Abdominal Hypertension
17 0 13 9.2E-02 0 0
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
164 0 25 9.1E-02 0 0
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
255 0 32 8.9E-02 0 0
CUI: C3714542
Disease: Lymphoma, Diffuse
Lymphoma, Diffuse
49 0 15 8.8E-02 0 0
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome
163 0 24 8.7E-02 0 0
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy
65 0 16 8.6E-02 0 0
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion
15 0 12 8.6E-02 0 0
CUI: C4285716
Disease: Melatonin deficiency
Melatonin deficiency
16 0 12 8.5E-02 0 0
CUI: C0005129
Disease: Bernard-Soulier Syndrome
Bernard-Soulier Syndrome
46 0 14 8.3E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1
46 0 14 8.3E-02 0 0