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 8 2.0E-03 0 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 4 9.8E-04 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 6 1.5E-03 0 0
CUI: C4305140
Disease: 12q14 microdeletion syndrome
12q14 microdeletion syndrome
2 0 1 2.5E-04 0 0
CUI: C3697269
Disease: 15q24 Microdeletion
15q24 Microdeletion
4 0 1 2.5E-04 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
1 0 1 2.5E-04 0 0
CUI: C3277849
Disease: 17,20-Lyase Deficiency, Isolated
17,20-Lyase Deficiency, Isolated
1 0 1 2.5E-04 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 4 9.8E-04 0 0
17-Hydroxysteroid Dehydrogenase Deficiency
5 0 1 2.5E-04 0 0
CUI: C4274528
Disease: 1q41q42 microdeletion syndrome
1q41q42 microdeletion syndrome
4 0 1 2.5E-04 0 0
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis
6 0 2 4.9E-04 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
1 0 1 2.5E-04 0 0
CUI: C3266731
Disease: 2-methyl-3-hydroxybutyric aciduria
2-methyl-3-hydroxybutyric aciduria
8 0 2 4.9E-04 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 36 8.8E-03 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
27 2 10 2.4E-03 1 1.0E-03
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
4 0 1 2.5E-04 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
14 0 5 1.2E-03 0 0
CUI: C4304531
Disease: 2q32q33 microdeletion syndrome
2q32q33 microdeletion syndrome
2 0 1 2.5E-04 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 3 7.4E-04 0 0
3-@METHYLGLUTACONIC ACIDURIA, TYPE I
2 0 1 2.5E-04 0 0
3-@METHYLGLUTACONIC ACIDURIA, TYPE V
3 0 1 2.5E-04 0 0
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
5 0 1 2.5E-04 0 0
3-Hydroxyacyl-CoA Dehydrogenase Deficiency
3 0 2 4.9E-04 0 0
3-methylcrotonyl CoA carboxylase 1 deficiency
5 0 3 7.4E-04 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
16 0 2 4.9E-04 0 0