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: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 0 1 9.8E-03 0 0
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis
6 0 1 1.1E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 6.0E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 7.3E-03 0 0
3-@METHYLGLUTACONIC ACIDURIA, TYPE V
3 0 1 1.2E-02 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
20 0 2 2.0E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 4 3.7E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3
12 0 3 3.3E-02 0 0
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
4 0 1 1.2E-02 0 0
46, XX Testicular Disorders of Sex Development
11 0 1 1.1E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 9.0E-03 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 2 1.9E-02 0 0
CUI: C3669122
Disease: 5-Alpha Reductase Deficiency
5-Alpha Reductase Deficiency
8 0 1 1.1E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 7.9E-03 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 2 1.7E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 5.4E-03 0 0
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute
2 0 1 1.2E-02 0 0
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions
6 0 1 1.1E-02 0 0
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
8 0 1 1.1E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 1.1E-02 0 0
Abdominal obesity metabolic syndrome
10 0 2 2.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 7 1.9E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 1.1E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 7 5.0E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 4 3.3E-02 0 0