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: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 0.33 0 0
CUI: C0346328
Disease: Meningioma of optic nerve sheath
Meningioma of optic nerve sheath 		1 0 1 0.33 0 0
CUI: C0349529
Disease: Gastric Carcinoid Tumor
Gastric Carcinoid Tumor 		1 0 1 0.33 0 0
CUI: C0584983
Disease: Homozygous Factor V Leiden mutation
Homozygous Factor V Leiden mutation 		1 0 1 0.33 0 0
CUI: C0678053
Disease: Stage IV Adrenal Cortex Carcinoma AJCC v7
Stage IV Adrenal Cortex Carcinoma AJCC v7 		1 0 1 0.33 0 0
CUI: C0940958
Disease: angioectasia
angioectasia 		1 0 1 0.33 0 0
CUI: C1142442
Disease: Intrahepatic biloma
Intrahepatic biloma 		1 0 1 0.33 0 0
CUI: C3203356
Disease: Factor II deficiency
Factor II deficiency 		1 0 1 0.33 0 0
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2 		1 0 1 0.33 0 0
CUI: C3890031
Disease: prothrombin type 3 phenotype
prothrombin type 3 phenotype 		1 0 1 0.33 0 0
CUI: C4016343
Disease: DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II
DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II 		1 0 1 0.33 0 0
CUI: C4021097
Disease: Reduced prothrombin activity
Reduced prothrombin activity 		1 0 1 0.33 0 0
CUI: C4518348
Disease: Ectopic pituitary adenoma
Ectopic pituitary adenoma 		1 0 1 0.33 0 0
CUI: C4693546
Disease: NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS
NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS 		1 0 1 0.33 0 0
CUI: C4693550
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59 		1 0 1 0.33 0 0
CUI: C4722227
Disease: Hypoprothrombinemias
Hypoprothrombinemias 		1 0 1 0.33 0 0
CUI: C0007093
Disease: Carcinoid Heart Disease
Carcinoid Heart Disease 		2 0 1 0.25 0 0
CUI: C0013288
Disease: Dumping Syndrome
Dumping Syndrome 		2 0 1 0.25 0 0
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		2 0 1 0.25 0 0
CUI: C0221243
Disease: Necrolytic Migratory Erythema
Necrolytic Migratory Erythema 		2 0 1 0.25 0 0
CUI: C0259744
Disease: dysproteinemia
dysproteinemia 		2 0 1 0.25 0 0
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		2 0 1 0.25 0 0
CUI: C0342569
Disease: Carcinoid crisis
Carcinoid crisis 		2 0 1 0.25 0 0
CUI: C0496901
Disease: Benign neoplasm of pituitary gland
Benign neoplasm of pituitary gland 		2 0 1 0.25 0 0
CUI: C0749087
Disease: Thrombosis of subclavian vein
Thrombosis of subclavian vein 		2 0 1 0.25 0 0