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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		0 4 0 0 1 6.2E-02
CUI: C0002894
Disease: Refractory anaemia with excess blasts
Refractory anaemia with excess blasts 		0 2 0 0 2 0.15
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 7.7E-02
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 7.7E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		0 8 0 0 2 0.11
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 7.7E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 7.7E-02
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		0 5 0 0 1 5.9E-02
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		0 3 0 0 1 6.7E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 2 0.15
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 0.15
CUI: C3150730
Disease: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY 		0 24 0 0 1 2.8E-02
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.3E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 1.0E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 3.8E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		94 0 1 6.8E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 1.4E-02 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		130 0 1 5.5E-03 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		24 0 1 1.3E-02 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 1 6.1E-03 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma 		8 0 1 1.7E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 1.6E-02 1 6.2E-02
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases 		13 0 1 1.5E-02 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 1 1.6E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 1.1E-02 0 0