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: C0238062
Disease: Chronic intestinal pseudo-obstruction
Chronic intestinal pseudo-obstruction 		0 10 0 0 1 2.6E-02
CUI: C0007462
Disease: Causalgia
Causalgia 		1 0 1 2.2E-02 0 0
CUI: C0032298
Disease: Pneumonia, Lipid
Pneumonia, Lipid 		1 0 1 2.2E-02 0 0
CUI: C0040213
Disease: Tietze's Syndrome
Tietze's Syndrome 		1 0 1 2.2E-02 0 0
CUI: C0153445
Disease: Malignant neoplasm of anal canal
Malignant neoplasm of anal canal 		1 0 1 2.2E-02 0 0
CUI: C0221385
Disease: Syphilitic gumma
Syphilitic gumma 		1 0 1 2.2E-02 0 0
CUI: C0238409
Disease: Renal Pelvis Squamous Cell Carcinoma
Renal Pelvis Squamous Cell Carcinoma 		1 0 1 2.2E-02 0 0
CUI: C0238479
Disease: Transient osteoporosis of hip
Transient osteoporosis of hip 		1 0 1 2.2E-02 0 0
CUI: C0265512
Disease: Bone island
Bone island 		1 0 1 2.2E-02 0 0
CUI: C0265978
Disease: Collagen nevus of skin
Collagen nevus of skin 		1 0 1 2.2E-02 0 0
CUI: C0270739
Disease: Hemichorea
Hemichorea 		1 0 1 2.2E-02 0 0
CUI: C0271347
Disease: Cavernous sinus syndrome
Cavernous sinus syndrome 		1 0 1 2.2E-02 0 0
CUI: C0278993
Disease: Recurrent Salivary Gland Cancer
Recurrent Salivary Gland Cancer 		1 0 1 2.2E-02 0 0
CUI: C0280266
Disease: stage, vulvar cancer
stage, vulvar cancer 		1 0 1 2.2E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 2.2E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 2.2E-02 0 0
CUI: C0341714
Disease: Lymphoma of kidney
Lymphoma of kidney 		1 0 1 2.2E-02 0 0
CUI: C0343524
Disease: Disseminated nocardiosis
Disseminated nocardiosis 		1 0 1 2.2E-02 0 0
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
Gorlin Chaudhry Moss syndrome 		1 0 1 2.2E-02 0 0
CUI: C0346082
Disease: Skin Lymphangiosarcoma
Skin Lymphangiosarcoma 		1 0 1 2.2E-02 0 0
CUI: C0346564
Disease: Carcinoma of base of tongue
Carcinoma of base of tongue 		1 0 1 2.2E-02 0 0
CUI: C0392464
Disease: Ventricular aneurysm
Ventricular aneurysm 		1 0 1 2.2E-02 0 0
CUI: C0431379
Disease: Laminar heterotopia
Laminar heterotopia 		1 0 1 2.2E-02 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 2.2E-02 0 0
CUI: C0454594
Disease: Surface dyslexia
Surface dyslexia 		1 0 1 2.2E-02 0 0