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: C3897877
Disease: Post-Hemorrhagic Hydrocephalus
Post-Hemorrhagic Hydrocephalus 		9 0 2 7.4E-02 0 0
CUI: C4551633
Disease: Pigmentary retinal dystrophy
Pigmentary retinal dystrophy 		9 0 2 7.4E-02 0 0
CUI: C4552482
Disease: CSSSI
CSSSI 		9 0 2 7.4E-02 0 0
CUI: C0268468
Disease: Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency 		10 0 2 7.1E-02 0 0
CUI: C0586989
Disease: Varicella Zoster Virus Infection
Varicella Zoster Virus Infection 		10 0 2 7.1E-02 0 0
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		10 0 2 7.1E-02 0 0
CUI: C3203657
Disease: Autoimmune retinopathy
Autoimmune retinopathy 		10 0 2 7.1E-02 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 0 2 6.9E-02 0 0
CUI: C0006444
Disease: Bursitis
Bursitis 		12 0 2 6.7E-02 0 0
CUI: C0154822
Disease: Serous retinal detachment
Serous retinal detachment 		12 0 2 6.7E-02 0 0
CUI: C0268425
Disease: Alstrom Syndrome
Alstrom Syndrome 		12 0 2 6.7E-02 0 0
CUI: C0149875
Disease: Primary dysmenorrhea
Primary dysmenorrhea 		13 0 2 6.5E-02 0 0
CUI: C0276926
Disease: Schistosoma hematobium infection
Schistosoma hematobium infection 		13 0 2 6.5E-02 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 2 6.5E-02 0 0
CUI: C4075603
Disease: Occult chronic type B viral hepatitis
Occult chronic type B viral hepatitis 		13 0 2 6.5E-02 0 0
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		30 0 3 6.4E-02 0 0
CUI: C1368911
Disease: Papillary urothelial carcinoma
Papillary urothelial carcinoma 		14 0 2 6.2E-02 0 0
CUI: C1846545
Disease: Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B 		14 0 2 6.2E-02 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 2 6.2E-02 0 0
CUI: C3888523
Disease: Autoimmune uveitis
Autoimmune uveitis 		31 0 3 6.2E-02 0 0
CUI: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation 		14 0 2 6.2E-02 0 0
CUI: C0334267
Disease: Transitional cell carcinoma in situ
Transitional cell carcinoma in situ 		15 0 2 6.1E-02 0 0
CUI: C0683381
Disease: inflammatory joint disease
inflammatory joint disease 		33 0 3 6.0E-02 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 2 5.9E-02 0 0
CUI: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		35 0 3 5.8E-02 0 0