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: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia
0 6 0 0 1 1.7E-03
CUI: C0268344
Disease: Ehlers-Danlos syndrome 6B
Ehlers-Danlos syndrome 6B
0 4 0 0 1 1.7E-03
CUI: C4551722
Disease: Encephalocele
Encephalocele
0 7 0 0 1 1.7E-03
CUI: C0007862
Disease: Cervico-Brachial Neuralgia
Cervico-Brachial Neuralgia
1 0 1 4.9E-03 0 0
CUI: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct
1 0 1 4.9E-03 0 0
CUI: C0039614
Disease: Tetanus
Tetanus
1 0 1 4.9E-03 0 0
CUI: C0085920
Disease: Brachial Neuralgia
Brachial Neuralgia
1 0 1 4.9E-03 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia
1 0 1 4.9E-03 0 0
CUI: C0155116
Disease: Descemet's membrane fold
Descemet's membrane fold
1 0 1 4.9E-03 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities
1 0 1 4.9E-03 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur
1 0 1 4.9E-03 0 0
CUI: C0264436
Disease: Mixed dust pneumoconiosis
Mixed dust pneumoconiosis
1 0 1 4.9E-03 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery
1 0 1 4.9E-03 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm
1 0 1 4.9E-03 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth
1 0 1 4.9E-03 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction
1 0 1 4.9E-03 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia
1 0 1 4.9E-03 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome
1 0 1 4.9E-03 0 0
Yellow mutant oculocutaneous albinism
1 0 1 4.9E-03 0 0
Impairment level: total impairment of both eyes (disorder)
1 0 1 4.9E-03 0 0
CUI: C0271651
Disease: Impaired glucose tolerance in obese
Impaired glucose tolerance in obese
1 0 1 4.9E-03 0 0
CUI: C0278679
Disease: Renal cell carcinoma recurrent
Renal cell carcinoma recurrent
1 0 1 4.9E-03 0 0
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation
1 0 1 4.9E-03 0 0
CUI: C0339681
Disease: Index myopia
Index myopia
1 0 1 4.9E-03 0 0
CUI: C0345002
Disease: Quadricuspid aortic valve
Quadricuspid aortic valve
1 0 1 4.9E-03 0 0