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: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 6.7E-02 0 0
CUI: C0006386
Disease: Bunion
Bunion 		1 0 1 6.7E-02 0 0
CUI: C0014574
Disease: Epiphysitis
Epiphysitis 		1 0 1 6.7E-02 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 6.7E-02 0 0
CUI: C0027095
Disease: Myosarcoma
Myosarcoma 		1 0 1 6.7E-02 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 6.7E-02 0 0
CUI: C0033579
Disease: Prostate nodule
Prostate nodule 		1 0 1 6.7E-02 0 0
CUI: C0036917
Disease: Sexually Transmitted Diseases, Bacterial
Sexually Transmitted Diseases, Bacterial 		1 0 1 6.7E-02 0 0
CUI: C0037018
Disease: Shwartzman Phenomenon
Shwartzman Phenomenon 		1 0 1 6.7E-02 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma 		1 0 1 6.7E-02 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication 		1 0 1 6.7E-02 0 0
CUI: C0153261
Disease: Histoplasma capsulatum Infection
Histoplasma capsulatum Infection 		1 0 1 6.7E-02 0 0
CUI: C0154565
Disease: Non-organic sleep disorder
Non-organic sleep disorder 		1 0 1 6.7E-02 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 6.7E-02 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation 		1 0 1 6.7E-02 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe 		1 0 1 6.7E-02 0 0
CUI: C0238309
Disease: Ischemic peripheral neuropathy
Ischemic peripheral neuropathy 		1 0 1 6.7E-02 0 0
CUI: C0238814
Disease: brain hemangioma
brain hemangioma 		1 0 1 6.7E-02 0 0
CUI: C0240812
Disease: Prostatic pain
Prostatic pain 		1 0 1 6.7E-02 0 0
CUI: C0262509
Disease: herpetic neuralgia
herpetic neuralgia 		1 0 1 6.7E-02 0 0
CUI: C0262981
Disease: Interface dermatitis
Interface dermatitis 		1 0 1 6.7E-02 0 0
CUI: C0263506
Disease: Perifolliculitis capitis abscedens
Perifolliculitis capitis abscedens 		1 0 1 6.7E-02 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 6.7E-02 0 0
CUI: C0265831
Disease: Congenital absence of pulmonic valve
Congenital absence of pulmonic valve 		1 0 1 6.7E-02 0 0
CUI: C0266782
Disease: Abnormal yolk sac
Abnormal yolk sac 		1 0 1 6.7E-02 0 0