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: C4022868
Disease: Abnormal circle of Willis morphology
Abnormal circle of Willis morphology 		4 0 4 0.50 0 0
CUI: C2713497
Disease: Saccular Aneurysm
Saccular Aneurysm 		5 0 4 0.44 0 0
CUI: C1862932
Disease: ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)
ANEURYSM, INTRACRANIAL BERRY, 1 (disorder) 		6 0 4 0.40 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		2 0 2 0.25 0 0
CUI: C1857693
Disease: Arteriovenous fistulas of celiac and mesenteric vessels
Arteriovenous fistulas of celiac and mesenteric vessels 		2 0 2 0.25 0 0
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology 		21 0 4 0.16 0 0
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		22 0 4 0.15 0 0
CUI: C4021971
Disease: Peripheral arteriovenous fistula
Peripheral arteriovenous fistula 		8 0 2 0.14 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 0.12 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 0.12 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 0.12 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		1 0 1 0.12 0 0
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		1 0 1 0.12 0 0
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		1 0 1 0.12 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 0.12 0 0
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		1 0 1 0.12 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 0.12 0 0
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		1 0 1 0.12 0 0
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		1 0 1 0.12 0 0
CUI: C1390214
Disease: Internal hemorrhage
Internal hemorrhage 		1 0 1 0.12 0 0
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		1 0 1 0.12 0 0
CUI: C1848795
Disease: GRAVES DISEASE, SUSCEPTIBILITY TO, 1
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 		1 0 1 0.12 0 0
CUI: C1851811
Disease: Hypermobility of distal interphalangeal joints
Hypermobility of distal interphalangeal joints 		1 0 1 0.12 0 0
CUI: C1853365
Disease: AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1 		1 0 1 0.12 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 0.12 0 0