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 2.6E-02 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 2.6E-02 0 0
CUI: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 2.6E-02 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 2 1 2.6E-02 2 0.13
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.6E-02 0 0
CUI: C0152422
Disease: Congenital aphakia
Congenital aphakia 		1 0 1 2.6E-02 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 2 1 2.6E-02 2 0.13
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 2.6E-02 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 2.6E-02 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 2.6E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 2.6E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 2.6E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 2.6E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 2.6E-02 0 0
CUI: C0269014
Disease: Fibrosis of corpus cavernosum
Fibrosis of corpus cavernosum 		1 0 1 2.6E-02 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 2.6E-02 0 0
CUI: C0302883
Disease: SMITH DISEASE
SMITH DISEASE 		1 0 1 2.6E-02 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 2.6E-02 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 2.6E-02 0 0
CUI: C0345982
Disease: Multiple self-healing epithelioma of Ferguson-Smith
Multiple self-healing epithelioma of Ferguson-Smith 		1 0 1 2.6E-02 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 2.6E-02 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 2.6E-02 0 0
CUI: C0410654
Disease: Instability of atlantooccipital joint
Instability of atlantooccipital joint 		1 0 1 2.6E-02 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation 		1 0 1 2.6E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 2.6E-02 0 0