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: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency 		3 0 2 0.18 0 0
CUI: C2609079
Disease: Mirror syndrome
Mirror syndrome 		4 0 2 0.17 0 0
CUI: C0596298
Disease: Cerebrovascular Occlusion
Cerebrovascular Occlusion 		9 0 2 0.12 0 0
CUI: C0011263
Disease: Multi-infarct dementia
Multi-infarct dementia 		30 0 4 0.11 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 1.0E-01 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse 		1 0 1 1.0E-01 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 1.0E-01 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 1.0E-01 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration 		1 0 1 1.0E-01 0 0
CUI: C0333319
Disease: Involucrum
Involucrum 		1 0 1 1.0E-01 0 0
CUI: C0339678
Disease: Simple myopia
Simple myopia 		1 0 1 1.0E-01 0 0
CUI: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		1 0 1 1.0E-01 0 0
CUI: C0344487
Disease: Lateral meningocele
Lateral meningocele 		1 0 1 1.0E-01 0 0
CUI: C0423693
Disease: Growing pains
Growing pains 		1 0 1 1.0E-01 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 1.0E-01 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 1.0E-01 0 0
CUI: C0748534
Disease: sciatic nerve inflammation
sciatic nerve inflammation 		1 0 1 1.0E-01 0 0
CUI: C1096352
Disease: Pancreatic enlargement
Pancreatic enlargement 		1 0 1 1.0E-01 0 0
CUI: C1142239
Disease: Call-Fleming syndrome
Call-Fleming syndrome 		1 0 1 1.0E-01 0 0
CUI: C1399357
Disease: Hemiparaesthesia
Hemiparaesthesia 		1 0 1 1.0E-01 0 0
CUI: C1832167
Disease: Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism
Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism 		1 0 1 1.0E-01 0 0
CUI: C1868414
Disease: HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C2748545
Disease: QUESTION MARK EARS, ISOLATED
QUESTION MARK EARS, ISOLATED 		1 0 1 1.0E-01 0 0
CUI: C2751494
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT 		1 0 1 1.0E-01 0 0
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		1 0 1 1.0E-01 0 0