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: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 5.3E-02 0 0
CUI: C0041915
Disease: Urachal Cyst
Urachal Cyst 		1 0 1 5.3E-02 0 0
CUI: C0234229
Disease: Deep pain
Deep pain 		1 0 1 5.3E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 5.3E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 5.3E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 5.3E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 5.3E-02 0 0
CUI: C0311343
Disease: Membranous conjunctivitis
Membranous conjunctivitis 		1 0 1 5.3E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 5.3E-02 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 5.3E-02 0 0
CUI: C0346363
Disease: Nevus of conjunctiva
Nevus of conjunctiva 		1 0 1 5.3E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 5.3E-02 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 5.3E-02 0 0
CUI: C0403639
Disease: Chemical cystitis
Chemical cystitis 		1 0 1 5.3E-02 0 0
CUI: C0423772
Disease: Cutaneous Fistula
Cutaneous Fistula 		1 0 1 5.3E-02 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 1 1 5.3E-02 1 0.33
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 5.3E-02 0 0
CUI: C0574014
Disease: Axillary vein thrombosis
Axillary vein thrombosis 		1 0 1 5.3E-02 0 0
CUI: C0854084
Disease: Streptococcal necrotizing fasciitis
Streptococcal necrotizing fasciitis 		1 0 1 5.3E-02 0 0
CUI: C1268937
Disease: Diarrhea-negative hemolytic uremic syndrome
Diarrhea-negative hemolytic uremic syndrome 		1 0 1 5.3E-02 0 0
CUI: C1274355
Disease: Streptococcal infection of skin
Streptococcal infection of skin 		1 0 1 5.3E-02 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 5.3E-02 0 0
CUI: C1319183
Disease: Corticosteroid induced cataract
Corticosteroid induced cataract 		1 0 1 5.3E-02 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 0 1 5.3E-02 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria 		1 0 1 5.3E-02 0 0