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: C0013421
Disease: Dystonia
Dystonia 		0 97 0 0 1 9.4E-03
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0 87 0 0 1 1.0E-02
CUI: C0035220
Disease: Respiratory Distress Syndrome, Newborn
Respiratory Distress Syndrome, Newborn 		0 37 0 0 1 2.2E-02
CUI: C0150055
Disease: Chronic pain
Chronic pain 		0 19 0 0 1 3.6E-02
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0 111 0 0 1 8.3E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.0E-01
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		0 37 0 0 1 2.2E-02
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		0 3 0 0 1 8.3E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.0E-01
CUI: C0852711
Disease: Sickle Cell Dactylitis
Sickle Cell Dactylitis 		0 7 0 0 1 6.2E-02
CUI: C3642345
Disease: Luminal A Breast Carcinoma
Luminal A Breast Carcinoma 		0 11 0 0 1 5.0E-02
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		0 4 0 0 1 7.7E-02
CUI: C0029106
Disease: Opisthorchiasis
Opisthorchiasis 		1 0 1 0.17 0 0
CUI: C0152097
Disease: Disease of diaphragm
Disease of diaphragm 		1 0 1 0.17 0 0
CUI: C0277004
Disease: Opisthorchis felineus Infection
Opisthorchis felineus Infection 		1 0 1 0.17 0 0
CUI: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 0.17 0 0
CUI: C1096494
Disease: Gastroduodenal haemorrhage
Gastroduodenal haemorrhage 		1 0 1 0.17 0 0
CUI: C1843832
Disease: VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 		1 0 1 0.17 0 0
CUI: C2677101
Disease: Inflammatory Bowel Disease 13
Inflammatory Bowel Disease 13 		1 0 1 0.17 0 0
CUI: C2718087
Disease: Vitamin K Deficiency Bleeding
Vitamin K Deficiency Bleeding 		1 0 1 0.17 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 0 1 0.17 0 0
CUI: C4054892
Disease: Grade II Chondrosarcoma
Grade II Chondrosarcoma 		1 0 1 0.17 0 0
CUI: C0030922
Disease: Peptic Ulcer Hemorrhage
Peptic Ulcer Hemorrhage 		2 0 1 0.14 0 0
CUI: C0040715
Disease: Chromosomal translocation
Chromosomal translocation 		2 0 1 0.14 0 0
CUI: C0206730
Disease: Neurothekeoma
Neurothekeoma 		2 0 2 0.33 0 0