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: C2936791
Disease: Antley-Bixler Syndrome, Autosomal Dominant
Antley-Bixler Syndrome, Autosomal Dominant 		9 0 4 0.25 0 0
CUI: C2676500
Disease: COWDEN-LIKE SYNDROME (disorder)
COWDEN-LIKE SYNDROME (disorder) 		5 0 3 0.23 0 0
CUI: C1959620
Disease: Dihydropyrimidine Dehydrogenase Deficiency
Dihydropyrimidine Dehydrogenase Deficiency 		7 0 3 0.20 0 0
CUI: C0220724
Disease: CONSTRICTING BANDS, CONGENITAL
CONSTRICTING BANDS, CONGENITAL 		16 0 4 0.17 0 0
CUI: C0338457
Disease: Aphasia, Progressive
Aphasia, Progressive 		10 0 3 0.17 0 0
CUI: C0235575
Disease: Hemolytic reaction
Hemolytic reaction 		4 0 2 0.15 0 0
CUI: C0338445
Disease: Familial Alzheimer's disease of early onset
Familial Alzheimer's disease of early onset 		14 0 3 0.14 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 2 0.13 0 0
CUI: C0031306
Disease: Phagocyte Bactericidal Dysfunction
Phagocyte Bactericidal Dysfunction 		7 0 2 0.12 0 0
CUI: C3661525
Disease: Autosomal Recessive Chronic Granulomatous Disease
Autosomal Recessive Chronic Granulomatous Disease 		7 0 2 0.12 0 0
CUI: C4021737
Disease: Chromosomal breakage induced by crosslinking agents
Chromosomal breakage induced by crosslinking agents 		8 0 2 0.12 0 0
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
Methylenetetrahydrofolate reductase polymorphism 		9 7 2 0.11 1 5.0E-02
CUI: C3826743
Disease: Anemia in children
Anemia in children 		9 0 2 0.11 0 0
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase 		10 63 2 0.11 1 1.3E-02
CUI: C0233407
Disease: Disorientation
Disorientation 		12 0 2 9.5E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 9.1E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 9.1E-02 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 9.1E-02 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		1 1 1 9.1E-02 1 7.1E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		1 1 1 9.1E-02 1 7.1E-02
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 9.1E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 9.1E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 9.1E-02 0 0
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		1 1 1 9.1E-02 1 7.1E-02
CUI: C0349661
Disease: Glial tumor of brain (disorder)
Glial tumor of brain (disorder) 		1 0 1 9.1E-02 0 0