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: C0749393
Disease: Chronic thrombocytopenia
Chronic thrombocytopenia 		1 0 1 4.5E-03 0 0
CUI: C0751445
Disease: Encephalitis, Polio
Encephalitis, Polio 		1 0 1 4.5E-03 0 0
CUI: C0751446
Disease: Poliomyelitis, Nonpoliovirus
Poliomyelitis, Nonpoliovirus 		1 0 1 4.5E-03 0 0
CUI: C0751447
Disease: Poliomyelitis, Preparalytic
Poliomyelitis, Preparalytic 		1 0 1 4.5E-03 0 0
CUI: C0795843
Disease: Chromosome 12 ring
Chromosome 12 ring 		1 0 1 4.5E-03 0 0
CUI: C0849850
Disease: Skin blotches
Skin blotches 		1 0 1 4.5E-03 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 4.5E-03 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 4.5E-03 0 0
CUI: C0948285
Disease: Corneal striae
Corneal striae 		1 0 1 4.5E-03 0 0
CUI: C1264000
Disease: Sickle cell-Hemoglobin O Arab disease
Sickle cell-Hemoglobin O Arab disease 		1 0 1 4.5E-03 0 0
CUI: C1272765
Disease: Minimal deviation adenocarcinoma of endocervical type
Minimal deviation adenocarcinoma of endocervical type 		1 0 1 4.5E-03 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 4.5E-03 0 0
CUI: C1275836
Disease: D - transposition of the great vessels
D - transposition of the great vessels 		1 0 1 4.5E-03 0 0
CUI: C1328928
Disease: Multiple Lentigines/LEOPARD syndrome
Multiple Lentigines/LEOPARD syndrome 		1 0 1 4.5E-03 0 0
CUI: C1332632
Disease: Breast Liposarcoma
Breast Liposarcoma 		1 0 1 4.5E-03 0 0
CUI: C1389901
Disease: Biotin-dependent carboxylase deficiency, unspecified
Biotin-dependent carboxylase deficiency, unspecified 		1 0 1 4.5E-03 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 0 1 4.5E-03 0 0
CUI: C1527258
Disease: Infantile paralysis
Infantile paralysis 		1 0 1 4.5E-03 0 0
CUI: C1709573
Disease: Pleural Epithelioid Hemangioendothelioma
Pleural Epithelioid Hemangioendothelioma 		1 0 1 4.5E-03 0 0
CUI: C1834345
Disease: Periosteal thickening of long tubular bones
Periosteal thickening of long tubular bones 		1 0 1 4.5E-03 0 0
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H 		1 0 1 4.5E-03 0 0
CUI: C1836823
Disease: Nephropathy with Pretibial Epidermolysis Bullosa and Deafness
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 		1 0 1 4.5E-03 0 0
CUI: C1847189
Disease: Absent scaphoid
Absent scaphoid 		1 0 1 4.5E-03 0 0
CUI: C1847711
Disease: NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO 		1 0 1 4.5E-03 0 0
CUI: C1848525
Disease: von Willebrand Disease, Recessive Form
von Willebrand Disease, Recessive Form 		1 0 1 4.5E-03 0 0