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: C4025774
Disease: 1-3 toe syndactyly
1-3 toe syndactyly
1 0 1 1.0E-02 0 0
CUI: C4023728
Disease: 1-5 finger syndactyly
1-5 finger syndactyly
3 0 1 1.0E-02 0 0
CUI: C4021235
Disease: 1-5 toe syndactyly
1-5 toe syndactyly
1 0 1 1.0E-02 0 0
CUI: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 3 2 1.7E-02 1 0.11
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 8 4.6E-02 0 0
2-oxo-hept-3-ene-1,7-dioate hydratase activity
14 0 1 9.1E-03 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 1 7.9E-03 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 1 9.3E-03 0 0
CUI: C4023115
Disease: 3-4 finger cutaneous syndactyly
3-4 finger cutaneous syndactyly
3 0 2 2.0E-02 0 0
CUI: C1856889
Disease: 3-4 finger syndactyly
3-4 finger syndactyly
4 0 1 1.0E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 1 7.9E-03 0 0
CUI: C1855126
Disease: 3-Methylglutaconic Aciduria Type IV
3-Methylglutaconic Aciduria Type IV
4 0 1 1.0E-02 0 0
3-Phosphoglycerate dehydrogenase deficiency
1 0 1 1.0E-02 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome
4 0 1 1.0E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 8.3E-03 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 7.1E-03 0 0
CUI: C4304526
Disease: 5q35 microduplication syndrome
5q35 microduplication syndrome
1 0 1 1.0E-02 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals
3 0 1 1.0E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 7.2E-03 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2
16 0 1 8.9E-03 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 1 9.5E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 5 1.3E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 9.5E-03 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 8.6E-03 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level
16 0 14 0.14 0 0