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: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 1.7E-02 0 0
CUI: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 1.7E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 1.7E-02 0 0
CUI: C0152422
Disease: Congenital aphakia
Congenital aphakia 		1 0 1 1.7E-02 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 1.7E-02 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 1.7E-02 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 1.7E-02 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 1.7E-02 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 1.7E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 1.7E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 1.7E-02 0 0
CUI: C0268356
Disease: Osteogenesis imperfecta with blue sclerae AND normal teeth
Osteogenesis imperfecta with blue sclerae AND normal teeth 		1 0 1 1.7E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 1.7E-02 0 0
CUI: C0269014
Disease: Fibrosis of corpus cavernosum
Fibrosis of corpus cavernosum 		1 0 1 1.7E-02 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 1.7E-02 0 0
CUI: C0302883
Disease: SMITH DISEASE
SMITH DISEASE 		1 0 1 1.7E-02 0 0
CUI: C0340235
Disease: Bronchobiliary fistula
Bronchobiliary fistula 		1 0 1 1.7E-02 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 1.7E-02 0 0
CUI: C0345982
Disease: Multiple self-healing epithelioma of Ferguson-Smith
Multiple self-healing epithelioma of Ferguson-Smith 		1 0 1 1.7E-02 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 1.7E-02 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 1.7E-02 0 0
CUI: C0410654
Disease: Instability of atlantooccipital joint
Instability of atlantooccipital joint 		1 0 1 1.7E-02 0 0
CUI: C0431709
Disease: Adult type polycystic kidney disease type 1
Adult type polycystic kidney disease type 1 		1 0 1 1.7E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 1.7E-02 0 0
CUI: C0519055
Disease: Renal involvement in scleroderma
Renal involvement in scleroderma 		1 0 1 1.7E-02 0 0