Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
(Idiopathic) normal pressure hydrocephalus
14 0 6 2.2E-03 0 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 2 7.5E-04 0 0
CUI: C4025774
Disease: 1-3 toe syndactyly
1-3 toe syndactyly
1 0 1 3.7E-04 0 0
CUI: C4023728
Disease: 1-5 finger syndactyly
1-5 finger syndactyly
3 0 1 3.7E-04 0 0
CUI: C4021235
Disease: 1-5 toe syndactyly
1-5 toe syndactyly
1 0 1 3.7E-04 0 0
CUI: C4476858
Disease: 1-minute APGAR score of 1
1-minute APGAR score of 1
1 0 1 3.7E-04 0 0
CUI: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 0 9 3.4E-03 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 2 7.5E-04 0 0
CUI: C4305140
Disease: 12q14 microdeletion syndrome
12q14 microdeletion syndrome
2 0 1 3.7E-04 0 0
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
7 0 2 7.5E-04 0 0
CUI: C3277849
Disease: 17,20-Lyase Deficiency, Isolated
17,20-Lyase Deficiency, Isolated
1 0 1 3.7E-04 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 2 7.5E-04 0 0
17-Hydroxysteroid Dehydrogenase Deficiency
5 0 1 3.7E-04 0 0
CUI: C4518822
Disease: 17q12 microdeletion syndrome
17q12 microdeletion syndrome
1 0 1 3.7E-04 0 0
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome
1 0 1 3.7E-04 0 0
CUI: C4304540
Disease: 1q44 microdeletion syndrome
1q44 microdeletion syndrome
1 0 1 3.7E-04 0 0
2,4-Dienoyl-CoA Reductase Deficiency
2 0 1 3.7E-04 0 0
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis
6 0 2 7.5E-04 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 18 6.6E-03 0 0
CUI: C4021622
Disease: 2-4 toe cutaneous syndactyly
2-4 toe cutaneous syndactyly
1 0 1 3.7E-04 0 0
CUI: C4021234
Disease: 2-4 toe syndactyly
2-4 toe syndactyly
2 0 1 3.7E-04 0 0
2-oxo-hept-3-ene-1,7-dioate hydratase activity
14 0 5 1.9E-03 0 0
CUI: C4304539
Disease: 20p12.3 microdeletion syndrome
20p12.3 microdeletion syndrome
1 0 1 3.7E-04 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 30 1.1E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 9 3.3E-03 0 0