Source: ALL
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: C1536168
Disease: Chronic pelvic pain syndrome
Chronic pelvic pain syndrome 		8 0 4 0.17 0 0
CUI: C0271073
Disease: Eales disease
Eales disease 		9 0 4 0.16 0 0
CUI: C3697010
Disease: Ulcerative colitis in remission
Ulcerative colitis in remission 		12 0 4 0.14 0 0
CUI: C0037933
Disease: Spinal Diseases
Spinal Diseases 		16 0 4 0.12 0 0
CUI: C4268599
Disease: Food-protein induced enterocolitis syndrome
Food-protein induced enterocolitis syndrome 		8 0 3 0.12 0 0
CUI: C0549379
Disease: Recurrent Carcinoma
Recurrent Carcinoma 		18 0 4 0.12 0 0
CUI: C0919746
Disease: Engraftment syndrome
Engraftment syndrome 		9 0 3 0.12 0 0
CUI: C4721438
Disease: Mitral valve dysplasia
Mitral valve dysplasia 		9 0 3 0.12 0 0
CUI: C4049431
Disease: Chronic hepatitis C genotype 4
Chronic hepatitis C genotype 4 		10 0 3 0.11 0 0
CUI: C0847614
Disease: Nasal allergies
Nasal allergies 		11 0 3 0.11 0 0
CUI: C0016782
Disease: Fuchs' heterochromic cyclitis
Fuchs' heterochromic cyclitis 		12 3 3 0.10 1 0.33
CUI: C0029877
Disease: Ear Inflammation
Ear Inflammation 		12 0 3 0.10 0 0
CUI: C0423673
Disease: Pain in spine
Pain in spine 		12 0 3 0.10 0 0
CUI: C0410438
Disease: Primary osteoporosis
Primary osteoporosis 		23 0 4 0.10 0 0
CUI: C0032962
Disease: Pregnancy Complications
Pregnancy Complications 		13 0 3 1.0E-01 0 0
CUI: C0038828
Disease: Superior Mesenteric Artery Syndrome
Superior Mesenteric Artery Syndrome 		2 0 2 1.0E-01 0 0
CUI: C0206178
Disease: Cytomegalovirus Retinitis
Cytomegalovirus Retinitis 		13 0 3 1.0E-01 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 1.0E-01 0 0
CUI: C0311276
Disease: Severe malnutrition
Severe malnutrition 		13 0 3 1.0E-01 0 0
CUI: C1321898
Disease: Blood in stool
Blood in stool 		13 0 3 1.0E-01 0 0
CUI: C1837593
Disease: Prostate Cancer, Hereditary, 4
Prostate Cancer, Hereditary, 4 		2 0 2 1.0E-01 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 2 1.0E-01 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 1.0E-01 0 0
CUI: C0029411
Disease: Osteoarthropathy, Primary Hypertrophic
Osteoarthropathy, Primary Hypertrophic 		14 0 3 9.7E-02 0 0
CUI: C0265808
Disease: Cyanotic congenital heart disease
Cyanotic congenital heart disease 		14 0 3 9.7E-02 0 0