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 1 7.5E-03 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 4.7E-03 0 0
2-oxo-hept-3-ene-1,7-dioate hydratase activity
14 0 1 7.1E-03 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 7.0E-03 0 0
CUI: C4023115
Disease: 3-4 finger cutaneous syndactyly
3-4 finger cutaneous syndactyly
3 0 1 7.7E-03 0 0
3-methylcrotonyl CoA carboxylase 1 deficiency
5 0 1 7.6E-03 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 4 2.4E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 1 6.1E-03 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 5.9E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 4.3E-03 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 7.6E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 2 1.3E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 7.1E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 14 3.4E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 2 1.4E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 7.8E-03 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci
7 0 3 2.3E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 7 3.8E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 3 2.1E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 2 1.2E-02 0 0
CUI: C4021208
Disease: Abnormal B cell count
Abnormal B cell count
2 0 2 1.6E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 21 2.1E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 3 1.5E-02 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 1 7.2E-03 0 0
CUI: C4476564
Disease: Abnormal brain lactate level by MRS
Abnormal brain lactate level by MRS
2 0 1 7.8E-03 0 0