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: C0021355
Disease: Infective otitis externa
Infective otitis externa 		1 0 1 0.25 0 0
CUI: C0157680
Disease: Carbuncle/furuncle
Carbuncle/furuncle 		1 0 1 0.25 0 0
CUI: C0238454
Disease: Cavernous Sinus Thrombosis
Cavernous Sinus Thrombosis 		1 0 1 0.25 0 0
CUI: C0259860
Disease: psychiatric emergencies
psychiatric emergencies 		1 0 1 0.25 0 0
CUI: C0578437
Disease: Ischemic foot
Ischemic foot 		1 0 1 0.25 0 0
CUI: C0854328
Disease: Infection due to anaerobic bacteria
Infection due to anaerobic bacteria 		1 0 1 0.25 0 0
CUI: C1333859
Disease: Grade 2 Colon Adenocarcinoma
Grade 2 Colon Adenocarcinoma 		1 0 1 0.25 0 0
CUI: C1846130
Disease: Mental retardation X-linked, South African type
Mental retardation X-linked, South African type 		1 0 1 0.25 0 0
CUI: C2349529
Disease: Pneumonia due to methicillin susceptible Staphylococcus aureus
Pneumonia due to methicillin susceptible Staphylococcus aureus 		1 0 1 0.25 0 0
CUI: C4021421
Disease: Abnormality of the proximal phalanx of the thumb
Abnormality of the proximal phalanx of the thumb 		1 0 1 0.25 0 0
CUI: C4310804
Disease: WITTEVEEN-KOLK SYNDROME
WITTEVEEN-KOLK SYNDROME 		1 0 1 0.25 0 0
CUI: C4540398
Disease: Thick ear helices
Thick ear helices 		1 0 1 0.25 0 0
CUI: C4552480
Disease: Complicated skin and skin structure infection
Complicated skin and skin structure infection 		1 0 1 0.25 0 0
CUI: C4706258
Disease: 2q33.1 microdeletion syndrome
2q33.1 microdeletion syndrome 		1 0 1 0.25 0 0
CUI: C0343525
Disease: Lemierre Syndrome
Lemierre Syndrome 		2 0 1 0.20 0 0
CUI: C0452221
Disease: Osteomyelitis of vertebra
Osteomyelitis of vertebra 		2 0 1 0.20 0 0
CUI: C0851881
Disease: Enterococcal infection
Enterococcal infection 		2 0 1 0.20 0 0
CUI: C1319193
Disease: Infection due to vancomycin resistant Staphylococcus aureus
Infection due to vancomycin resistant Staphylococcus aureus 		2 0 1 0.20 0 0
CUI: C1843228
Disease: Hypotrophy of the small hand muscles
Hypotrophy of the small hand muscles 		2 0 1 0.20 0 0
CUI: C1846133
Disease: Loss of ability to walk in first decade
Loss of ability to walk in first decade 		2 0 1 0.20 0 0
CUI: C2676739
Disease: Chromosome 2q32-Q33 Deletion Syndrome
Chromosome 2q32-Q33 Deletion Syndrome 		2 0 1 0.20 0 0
CUI: C2931713
Disease: Chromosome 17 deletion
Chromosome 17 deletion 		2 0 1 0.20 0 0
CUI: C3179058
Disease: Corpus Callosum Malformation
Corpus Callosum Malformation 		2 0 1 0.20 0 0
CUI: C3683846
Disease: Chromosome 17p Deletion Syndrome
Chromosome 17p Deletion Syndrome 		2 0 1 0.20 0 0
CUI: C4021770
Disease: Clinodactyly of toe
Clinodactyly of toe 		8 0 2 0.20 0 0