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: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 6.7E-02 0 0
CUI: C0152422
Disease: Congenital aphakia
Congenital aphakia 		1 0 1 6.7E-02 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 6.7E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 6.7E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 6.7E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 6.7E-02 0 0
CUI: C0269014
Disease: Fibrosis of corpus cavernosum
Fibrosis of corpus cavernosum 		1 0 1 6.7E-02 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 6.7E-02 0 0
CUI: C0302883
Disease: SMITH DISEASE
SMITH DISEASE 		1 0 1 6.7E-02 0 0
CUI: C0345982
Disease: Multiple self-healing epithelioma of Ferguson-Smith
Multiple self-healing epithelioma of Ferguson-Smith 		1 0 1 6.7E-02 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 6.7E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 6.7E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 6.7E-02 0 0
CUI: C0741621
Disease: Brachial artery occlusion
Brachial artery occlusion 		1 0 1 6.7E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 6.7E-02 0 0
CUI: C0857856
Disease: Staphylococcus aureus abscess
Staphylococcus aureus abscess 		1 0 1 6.7E-02 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 6.7E-02 0 0
CUI: C1303010
Disease: Mydriasis, Congenital
Mydriasis, Congenital 		1 0 1 6.7E-02 0 0
CUI: C1305147
Disease: Congenital supravalvular aortic stenosis
Congenital supravalvular aortic stenosis 		1 0 1 6.7E-02 0 0
CUI: C1336007
Disease: Small Intestinal Sarcoma
Small Intestinal Sarcoma 		1 0 1 6.7E-02 0 0
CUI: C1388201
Disease: Ascending aortic rupture
Ascending aortic rupture 		1 0 1 6.7E-02 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 6.7E-02 0 0
CUI: C1853234
Disease: Anterior segment of eye aplasia
Anterior segment of eye aplasia 		1 0 1 6.7E-02 0 0
CUI: C1860896
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6 		1 0 1 6.7E-02 0 0
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 0 1 6.7E-02 0 0