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: C0268351
Disease: Cutis Laxa, Autosomal Recessive, Type I
Cutis Laxa, Autosomal Recessive, Type I 		2 0 2 1.00 0 0
CUI: C0432336
Disease: Cutis laxa, recessive, type I
Cutis laxa, recessive, type I 		2 0 2 1.00 0 0
CUI: C2931134
Disease: Cutis laxa, recessive
Cutis laxa, recessive 		3 0 2 0.67 0 0
CUI: C1837187
Disease: MACULAR DEGENERATION, AGE-RELATED, 3
MACULAR DEGENERATION, AGE-RELATED, 3 		1 0 1 0.50 0 0
CUI: C4225406
Disease: NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION
NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION 		1 0 1 0.50 0 0
CUI: C4285705
Disease: Pulmonary artery occlusion
Pulmonary artery occlusion 		1 0 1 0.50 0 0
CUI: C4489482
Disease: Aneurysm or dissection
Aneurysm or dissection 		1 0 1 0.50 0 0
CUI: C1395674
Disease: Bowel diverticulosis
Bowel diverticulosis 		5 0 2 0.40 0 0
CUI: C2673776
Disease: Vascular tortuosity
Vascular tortuosity 		2 0 1 0.33 0 0
CUI: C2751321
Disease: Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 		2 0 1 0.33 0 0
CUI: C3280798
Disease: CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB 		2 0 1 0.33 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant 		3 0 1 0.25 0 0
CUI: C0406549
Disease: Cutis laxa, acquired type
Cutis laxa, acquired type 		3 0 1 0.25 0 0
CUI: C0155676
Disease: Pulmonary artery aneurysm
Pulmonary artery aneurysm 		4 0 1 0.20 0 0
CUI: C1836651
Disease: Generalized arterial tortuosity
Generalized arterial tortuosity 		4 0 1 0.20 0 0
CUI: C0037301
Disease: Skin Wrinkling
Skin Wrinkling 		12 0 2 0.17 0 0
CUI: C0265010
Disease: Ruptured thoracic aortic aneurysm
Ruptured thoracic aortic aneurysm 		5 0 1 0.17 0 0
CUI: C0265012
Disease: Ruptured abdominal aortic aneurysm
Ruptured abdominal aortic aneurysm 		5 0 1 0.17 0 0
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		5 0 1 0.17 0 0
CUI: C1305122
Disease: Thoracoabdominal aortic aneurysm, ruptured
Thoracoabdominal aortic aneurysm, ruptured 		5 0 1 0.17 0 0
CUI: C2749369
Disease: Prominence of the premaxilla
Prominence of the premaxilla 		5 0 1 0.17 0 0
CUI: C0038449
Disease: Stricture of artery
Stricture of artery 		16 0 2 0.12 0 0
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese 		7 0 1 0.12 0 0
CUI: C3665335
Disease: Cutis laxa, autosomal recessive
Cutis laxa, autosomal recessive 		17 0 2 0.12 0 0
CUI: C0156273
Disease: Bladder Diverticulum
Bladder Diverticulum 		18 0 2 0.11 0 0