Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
(Idiopathic) normal pressure hydrocephalus
14 0 1 4.5E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.6E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 2 3.8E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 2 4.4E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 1 3.8E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 4.0E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 2 7.4E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 2.0E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 3 3.3E-03 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 1 5.0E-02 0 0
CUI: C0278061
Disease: Abnormal mental state
Abnormal mental state
24 0 1 3.1E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
109 0 2 1.7E-02 0 0
CUI: C0000833
Disease: Abscess
Abscess
96 0 5 5.0E-02 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy
89 0 1 1.0E-02 0 0
CUI: C1456418
Disease: Absence of muscle
Absence of muscle
12 0 1 5.0E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation
111 0 1 8.4E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 1 4.7E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 4.2E-03 0 0
CUI: C4552483
Disease: ABSSSI
ABSSSI
2 0 1 1.0E-01 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 5.3E-02 0 0
CUI: C0221270
Disease: Acanthosis
Acanthosis
37 0 1 2.2E-02 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
64 0 1 1.4E-02 0 0
CUI: C0234238
Disease: Ache
Ache
50 0 1 1.7E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 0 1 1.9E-02 0 0