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: C0009759
Disease: Conjunctival Diseases
Conjunctival Diseases 		6 0 2 0.12 0 0
CUI: C0030824
Disease: Allergy to penicillin
Allergy to penicillin 		6 0 2 0.12 0 0
CUI: C0152068
Disease: Echinococcus granulosus infection
Echinococcus granulosus infection 		6 0 2 0.12 0 0
CUI: C0477474
Disease: Dermatitis and eczema
Dermatitis and eczema 		6 0 2 0.12 0 0
CUI: C0854359
Disease: Insulin autoimmune syndrome
Insulin autoimmune syndrome 		6 0 2 0.12 0 0
CUI: C1332655
Disease: Complement component 3 deficiency
Complement component 3 deficiency 		6 0 2 0.12 0 0
CUI: C1510449
Disease: Chronic iridocyclitis
Chronic iridocyclitis 		6 0 2 0.12 0 0
CUI: C1608955
Disease: Mycobacterium abscessus Infection
Mycobacterium abscessus Infection 		6 0 2 0.12 0 0
CUI: C2887821
Disease: Left sided colitis
Left sided colitis 		6 0 2 0.12 0 0
CUI: C3888521
Disease: Autoimmune demyelinating disease
Autoimmune demyelinating disease 		6 0 2 0.12 0 0
CUI: C0403396
Disease: Steroid-sensitive nephrotic syndrome
Steroid-sensitive nephrotic syndrome 		36 0 5 0.11 0 0
CUI: C0020522
Disease: Delayed Hypersensitivity
Delayed Hypersensitivity 		7 0 2 0.11 0 0
CUI: C0342158
Disease: Hypothyroidism, Autoimmune
Hypothyroidism, Autoimmune 		17 0 3 0.11 0 0
CUI: C0543698
Disease: Hypersensitive syndrome
Hypersensitive syndrome 		17 0 3 0.11 0 0
CUI: C0740842
Disease: AIDS related illness
AIDS related illness 		7 0 2 0.11 0 0
CUI: C1262147
Disease: Scleroderma renal crisis
Scleroderma renal crisis 		7 0 2 0.11 0 0
CUI: C1843273
Disease: Tubulointerstitial nephritis and uveitis
Tubulointerstitial nephritis and uveitis 		7 0 2 0.11 0 0
CUI: C3888318
Disease: Myopathy, familial idiopathic inflammatory
Myopathy, familial idiopathic inflammatory 		7 0 2 0.11 0 0
CUI: C4049279
Disease: Post stroke epilepsy
Post stroke epilepsy 		7 0 2 0.11 0 0
CUI: C0029295
Disease: Oropharyngeal Neoplasms
Oropharyngeal Neoplasms 		8 0 2 0.11 0 0
CUI: C0155880
Disease: Intrinsic asthma
Intrinsic asthma 		29 0 4 0.11 0 0
CUI: C0745242
Disease: Immunoglobulin deficiency
Immunoglobulin deficiency 		8 0 2 0.11 0 0
CUI: C0853602
Disease: Immunodeficiency congenital
Immunodeficiency congenital 		8 0 2 0.11 0 0
CUI: C1275465
Disease: Tumor stage mycosis fungoides
Tumor stage mycosis fungoides 		8 0 2 0.11 0 0
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		8 0 2 0.11 0 0