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: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 0.25 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 0.25 0 0
CUI: C0271285
Disease: Epithelial basement membrane dystrophy
Epithelial basement membrane dystrophy 		1 0 1 0.25 0 0
CUI: C0334083
Disease: Connective tissue nevus, NOS
Connective tissue nevus, NOS 		6 0 2 0.25 0 0
CUI: C0339271
Disease: Salzmann nodular dystrophy
Salzmann nodular dystrophy 		1 0 1 0.25 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 0.25 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 0.25 0 0
CUI: C0521723
Disease: Corneal dystrophy, epithelial basement membrane
Corneal dystrophy, epithelial basement membrane 		1 0 1 0.25 0 0
CUI: C1390214
Disease: Internal hemorrhage
Internal hemorrhage 		1 0 1 0.25 0 0
CUI: C1641846
Disease: Groenouw corneal dystrophy type I (disorder)
Groenouw corneal dystrophy type I (disorder) 		1 0 1 0.25 0 0
CUI: C1833699
Disease: Osteopoikilosis, Isolated
Osteopoikilosis, Isolated 		1 2 1 0.25 2 1.00
CUI: C1837974
Disease: Corneal Dystrophy, Lattice Type IIIA
Corneal Dystrophy, Lattice Type IIIA 		1 0 1 0.25 0 0
CUI: C1851811
Disease: Hypermobility of distal interphalangeal joints
Hypermobility of distal interphalangeal joints 		1 0 1 0.25 0 0
CUI: C1853365
Disease: AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1 		1 0 1 0.25 0 0
CUI: C2699508
Disease: Splenic diffuse red pulp small B-cell lymphoma
Splenic diffuse red pulp small B-cell lymphoma 		1 0 1 0.25 0 0
CUI: C2931505
Disease: Mixed sclerosing bone dystrophy
Mixed sclerosing bone dystrophy 		1 0 1 0.25 0 0
CUI: C3149399
Disease: DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED
DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED 		1 2 1 0.25 1 0.33
CUI: C3149695
Disease: Melorheostosis with Osteopoikilosis
Melorheostosis with Osteopoikilosis 		1 1 1 0.25 1 0.50
CUI: C3495371
Disease: Juvenile elastoma
Juvenile elastoma 		1 0 1 0.25 0 0
CUI: C3809006
Disease: CARDIOFACIOCUTANEOUS SYNDROME 3
CARDIOFACIOCUTANEOUS SYNDROME 3 		1 0 1 0.25 0 0
CUI: C4024118
Disease: Complete duplication of the distal phalanges of the hand
Complete duplication of the distal phalanges of the hand 		1 0 1 0.25 0 0
CUI: C4024792
Disease: Nodular corneal dystrophy
Nodular corneal dystrophy 		1 0 1 0.25 0 0
CUI: C4024796
Disease: Punctate corneal dystrophy
Punctate corneal dystrophy 		1 0 1 0.25 0 0
CUI: C4540530
Disease: EHLERS-DANLOS SYNDROME, NONVASCULAR VARIANT
EHLERS-DANLOS SYNDROME, NONVASCULAR VARIANT 		1 0 1 0.25 0 0
CUI: C0010035
Disease: Hereditary corneal dystrophy
Hereditary corneal dystrophy 		2 0 1 0.20 0 0