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: C0154089
Disease: Carcinoma in situ of penis
Carcinoma in situ of penis 		1 0 1 4.8E-03 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 4.8E-03 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 4.8E-03 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 4.8E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 4.8E-03 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 4.8E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 4.8E-03 0 0
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 0 1 4.8E-03 0 0
CUI: C0221385
Disease: Syphilitic gumma
Syphilitic gumma 		1 0 1 4.8E-03 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 4.8E-03 0 0
CUI: C0232495
Disease: Lower abdominal pain
Lower abdominal pain 		1 0 1 4.8E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 4.8E-03 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 4.8E-03 0 0
CUI: C0235146
Disease: Euphoric mood
Euphoric mood 		1 0 1 4.8E-03 0 0
CUI: C0238309
Disease: Ischemic peripheral neuropathy
Ischemic peripheral neuropathy 		1 0 1 4.8E-03 0 0
CUI: C0238409
Disease: Renal Pelvis Squamous Cell Carcinoma
Renal Pelvis Squamous Cell Carcinoma 		1 0 1 4.8E-03 0 0
CUI: C0238479
Disease: Transient osteoporosis of hip
Transient osteoporosis of hip 		1 0 1 4.8E-03 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 4.8E-03 0 0
CUI: C0238814
Disease: brain hemangioma
brain hemangioma 		1 0 1 4.8E-03 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 4.8E-03 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 4.8E-03 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 4.8E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 4.8E-03 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 4.8E-03 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 4.8E-03 0 0