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: C0549357
Disease: Abdominal adhesions
Abdominal adhesions
6 0 2 1.1E-02 0 0
CUI: C1142214
Disease: Abdominal cocoon
Abdominal cocoon
1 0 1 5.9E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 5.2E-03 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 2 1.1E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 3 1.7E-02 0 0
Abdominal obesity metabolic syndrome
10 0 1 5.6E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 30 6.8E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 1 5.3E-03 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 3 1.6E-02 0 0
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect
8 0 1 5.6E-03 0 0
CUI: C4551519
Disease: Abducens Nerve Palsy
Abducens Nerve Palsy
8 0 3 1.7E-02 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci
7 0 3 1.7E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 8.6E-03 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 3 1.4E-02 0 0
Abnormal atrioventricular conduction
7 0 2 1.1E-02 0 0
Abnormal B-type natriuretic peptide level
1 0 1 5.9E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 36 3.4E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 4 1.7E-02 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 2 1.1E-02 0 0
Abnormal brain FDG positron emission tomography
18 0 1 5.3E-03 0 0
CUI: C4476564
Disease: Abnormal brain lactate level by MRS
Abnormal brain lactate level by MRS
2 0 1 5.8E-03 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 1 5.5E-03 0 0
CUI: C4025680
Disease: Abnormal cartilage morphology
Abnormal cartilage morphology
2 0 1 5.8E-03 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 5.8E-03 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology
16 0 2 1.1E-02 0 0