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: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		8 0 3 7.9E-02 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 3 7.7E-02 0 0
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis 		53 0 6 7.5E-02 0 0
CUI: C0042166
Disease: Uveitis, Intermediate
Uveitis, Intermediate 		10 0 3 7.5E-02 0 0
CUI: C0232943
Disease: Intermenstrual heavy bleeding
Intermenstrual heavy bleeding 		10 0 3 7.5E-02 0 0
CUI: C1535942
Disease: Polyglandular Type III Autoimmune Syndrome
Polyglandular Type III Autoimmune Syndrome 		10 0 3 7.5E-02 0 0
CUI: C0263314
Disease: Pemphigus and fogo selvagem
Pemphigus and fogo selvagem 		26 0 4 7.3E-02 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		71 0 7 7.2E-02 0 0
CUI: C4477095
Disease: Increased lactate dehydrogenase activity
Increased lactate dehydrogenase activity 		27 0 4 7.1E-02 0 0
CUI: C0030343
Disease: Panuveitis
Panuveitis 		13 0 3 7.0E-02 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 3 7.0E-02 0 0
CUI: C1692871
Disease: Inflammatory polyarthritis
Inflammatory polyarthritis 		13 0 3 7.0E-02 0 0
CUI: C0029411
Disease: Osteoarthropathy, Primary Hypertrophic
Osteoarthropathy, Primary Hypertrophic 		14 0 3 6.8E-02 0 0
CUI: C0085860
Disease: Autoimmune Syndrome Type II, Polyglandular
Autoimmune Syndrome Type II, Polyglandular 		14 0 3 6.8E-02 0 0
CUI: C0521173
Disease: Granulomatosis
Granulomatosis 		14 0 3 6.8E-02 0 0
CUI: C0678202
Disease: Regional enteritis
Regional enteritis 		46 0 5 6.8E-02 0 0
CUI: C1864997
Disease: Majeed syndrome
Majeed syndrome 		15 0 3 6.7E-02 0 0
CUI: C0155502
Disease: Benign Paroxysmal Positional Vertigo
Benign Paroxysmal Positional Vertigo 		16 0 3 6.5E-02 0 0
CUI: C0032533
Disease: Polymyalgia Rheumatica
Polymyalgia Rheumatica 		51 0 5 6.3E-02 0 0
CUI: C0151436
Disease: Vasculitis, Leukocytoclastic, Cutaneous
Vasculitis, Leukocytoclastic, Cutaneous 		18 0 3 6.2E-02 0 0
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		53 0 5 6.2E-02 0 0
CUI: C0263505
Disease: Alopecia universalis
Alopecia universalis 		19 0 3 6.1E-02 0 0
CUI: C0345408
Disease: Hereditary clubbing
Hereditary clubbing 		2 0 2 6.1E-02 0 0
CUI: C1274377
Disease: Vibrio vulnificus infection
Vibrio vulnificus infection 		2 0 2 6.1E-02 0 0
CUI: C1409412
Disease: Periostosis
Periostosis 		2 0 2 6.1E-02 0 0