Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
21 24 12 0.24 12 0.29
CUI: C3873363
Disease: Acute pulmonary thromboembolism
Acute pulmonary thromboembolism
15 0 10 0.22 0 0
FANCONI ANEMIA, COMPLEMENTATION GROUP F
13 0 9 0.20 0 0
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion
15 0 9 0.19 0 0
CUI: C0276721
Disease: Phaeohyphomycosis
Phaeohyphomycosis
9 0 8 0.19 0 0
CUI: C0276279
Disease: Mink parvovirus infection
Mink parvovirus infection
10 0 8 0.19 0 0
CUI: C0017672
Disease: Glossalgia
Glossalgia
11 0 8 0.18 0 0
Chronic myeloid leukaemia transformation
11 0 8 0.18 0 0
CUI: C4546431
Disease: Exacerbation of allergic asthma
Exacerbation of allergic asthma
11 0 8 0.18 0 0
CUI: C0268251
Disease: Gaucher Disease, Type 3 (disorder)
Gaucher Disease, Type 3 (disorder)
18 0 9 0.18 0 0
CUI: C0406486
Disease: Ocular Rosacea
Ocular Rosacea
12 0 8 0.18 0 0
CUI: C0474368
Disease: Labor Pain
Labor Pain
12 0 8 0.18 0 0
CUI: C2721566
Disease: Meniscal degeneration
Meniscal degeneration
13 0 8 0.17 0 0
CUI: C0400807
Disease: Stress ulcer of stomach
Stress ulcer of stomach
14 0 8 0.17 0 0
CUI: C2741638
Disease: Stress ulcer
Stress ulcer
14 0 8 0.17 0 0
CUI: C1319466
Disease: Barber Say syndrome
Barber Say syndrome
21 0 9 0.17 0 0
CUI: C1864040
Disease: Cerebral Cavernous Malformations 3
Cerebral Cavernous Malformations 3
15 0 8 0.17 0 0
FANCONI ANEMIA, COMPLEMENTATION GROUP C
22 0 9 0.17 0 0
CUI: C0007192
Disease: Cardiomyopathy, Alcoholic
Cardiomyopathy, Alcoholic
30 0 10 0.16 0 0
CUI: C2242710
Disease: Intra-Abdominal Hypertension
Intra-Abdominal Hypertension
17 0 8 0.16 0 0
CUI: C0151565
Disease: Hemorrhagic colitis
Hemorrhagic colitis
18 0 8 0.16 0 0
CUI: C1455780
Disease: Aortic valve sclerosis
Aortic valve sclerosis
18 0 8 0.16 0 0
CUI: C0015974
Disease: Periodic fever
Periodic fever
19 0 8 0.15 0 0
CUI: C0428796
Disease: Senile sclerosis of aortic cusp
Senile sclerosis of aortic cusp
19 0 8 0.15 0 0
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1
19 0 8 0.15 0 0