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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 5.6E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.0E-01
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0 68 0 0 2 2.6E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		0 35 0 0 1 2.3E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		0 21 0 0 1 3.3E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 7.1E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.6E-03
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		0 144 0 0 1 6.5E-03
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		0 12 0 0 1 4.8E-02
CUI: C0919890
Disease: Hyperfibrinogenemia
Hyperfibrinogenemia 		0 1 0 0 1 1.0E-01
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0 19 0 0 1 3.6E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 4.5E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 8.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.0E-01
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.0E-01
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 9.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 5.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 8.3E-02
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 7.2E-03 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		188 0 1 4.5E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 1.2E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 4.1E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		94 0 1 7.7E-03 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 1 3.6E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 2.4E-02 0 0