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: C0585473
Disease: Chondromyxoid fibroma of bone
Chondromyxoid fibroma of bone 		1 0 1 0.12 0 0
CUI: C0751097
Disease: Empty Sella Syndrome, Secondary
Empty Sella Syndrome, Secondary 		1 0 1 0.12 0 0
CUI: C0849963
Disease: Feeling nervous
Feeling nervous 		1 0 1 0.12 0 0
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		1 0 1 0.12 0 0
CUI: C0856836
Disease: Systemic juvenile chronic arthritis
Systemic juvenile chronic arthritis 		1 0 1 0.12 0 0
CUI: C0878576
Disease: Posterior Leukoencephalopathy Syndrome
Posterior Leukoencephalopathy Syndrome 		1 0 1 0.12 0 0
CUI: C0948109
Disease: Idiopathic neutropenia
Idiopathic neutropenia 		1 0 1 0.12 0 0
CUI: C1290073
Disease: Acute mucositis
Acute mucositis 		1 0 1 0.12 0 0
CUI: C1335169
Disease: Ovarian Adenosarcoma
Ovarian Adenosarcoma 		1 0 1 0.12 0 0
CUI: C1641846
Disease: Groenouw corneal dystrophy type I (disorder)
Groenouw corneal dystrophy type I (disorder) 		1 3 1 0.12 3 0.50
CUI: C1832273
Disease: Ribbing disease
Ribbing disease 		1 0 1 0.12 0 0
CUI: C1835178
Disease: MACULAR DYSTROPHY, ATYPICAL VITELLIFORM
MACULAR DYSTROPHY, ATYPICAL VITELLIFORM 		1 0 1 0.12 0 0
CUI: C1837974
Disease: Corneal Dystrophy, Lattice Type IIIA
Corneal Dystrophy, Lattice Type IIIA 		1 6 1 0.12 3 0.33
CUI: C1851612
Disease: Narrowing of medullary canal
Narrowing of medullary canal 		1 0 1 0.12 0 0
CUI: C1866075
Disease: GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder) 		1 0 1 0.12 0 0
CUI: C1868990
Disease: Acute HIV syndrome
Acute HIV syndrome 		1 0 1 0.12 0 0
CUI: C2242510
Disease: Splenic varices
Splenic varices 		1 0 1 0.12 0 0
CUI: C2242653
Disease: Thyroid fibrosis
Thyroid fibrosis 		1 0 1 0.12 0 0
CUI: C2717859
Disease: Peritoneal Sclerosis
Peritoneal Sclerosis 		1 0 1 0.12 0 0
CUI: C3179037
Disease: Developmental Coxa Vara
Developmental Coxa Vara 		1 0 1 0.12 0 0
CUI: C3280099
Disease: CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME 		1 0 1 0.12 0 0
CUI: C3544328
Disease: Prostatic fibrosis
Prostatic fibrosis 		1 0 1 0.12 0 0
CUI: C3839737
Disease: High astigmatism
High astigmatism 		1 0 1 0.12 0 0
CUI: C4016044
Disease: SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC 		1 0 1 0.12 0 0
CUI: C4023332
Disease: Abnormal corneal endothelium morphology
Abnormal corneal endothelium morphology 		1 0 1 0.12 0 0