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: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 2 3.0E-02 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 1.4E-02 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
1 0 1 1.6E-02 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 2 3.1E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 6.8E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 2 1.7E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 2 3 3.3E-02 1 0.20
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 1 1.4E-02 0 0
2nd-5th toe middle phalangeal hypoplasia
2 0 1 1.6E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 1.4E-02 0 0
CUI: C1856889
Disease: 3-4 finger syndactyly
3-4 finger syndactyly
4 0 1 1.5E-02 0 0
CUI: C1834062
Disease: 3-4 toe syndactyly
3-4 toe syndactyly
4 0 1 1.5E-02 0 0
CUI: C1837836
Disease: 4-5 toe syndactyly
4-5 toe syndactyly
4 0 1 1.5E-02 0 0
CUI: C2936403
Disease: 46, XX Disorders of Sex Development
46, XX Disorders of Sex Development
6 0 1 1.5E-02 0 0
46, XX Testicular Disorders of Sex Development
11 0 1 1.4E-02 0 0
CUI: C0432481
Disease: 46, XX true hermaphrodite
46, XX true hermaphrodite
2 0 1 1.6E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 2 2.2E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 1.2E-02 0 0
46,Xy Gonadal Dysgenesis, Complete, Sry-Related
1 0 1 1.6E-02 0 0
CUI: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis
11 0 1 1.4E-02 0 0
46,Xy True Hermaphroditism, Sry-Related
1 0 1 1.6E-02 0 0
CUI: C3266843
Disease: 47, XYY syndrome
47, XYY syndrome
9 0 1 1.4E-02 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals
3 0 1 1.6E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 1 1.5E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 2 2.0E-02 0 0