Source: ALL
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 3 1.6E-02 0 0
CUI: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs 		20 0 1 4.8E-03 0 0
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement 		7 0 1 5.1E-03 0 0
CUI: C1150929
Disease: 2-oxo-hept-3-ene-1,7-dioate hydratase activity
2-oxo-hept-3-ene-1,7-dioate hydratase activity 		14 0 1 4.9E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		55 0 1 4.1E-03 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 1 4.5E-03 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female 		25 0 1 4.7E-03 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis 		38 0 10 4.6E-02 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess 		4 0 1 5.2E-03 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating 		10 0 3 1.5E-02 0 0
CUI: C1142110
Disease: Abdominal Compartment Syndrome
Abdominal Compartment Syndrome 		2 0 1 5.2E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection 		23 0 3 1.4E-02 0 0
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		10 0 1 5.0E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 16 3.4E-02 0 0
CUI: C3826804
Disease: Abdominal pain in children
Abdominal pain in children 		2 0 1 5.2E-03 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis 		18 0 3 1.5E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom 		17 0 2 9.8E-03 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness 		2 0 2 1.1E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis 		2 0 2 1.1E-02 0 0
CUI: C0919934
Disease: Abdominal wall infection
Abdominal wall infection 		1 0 1 5.3E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 2 7.9E-03 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon 		20 0 2 9.6E-03 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME 		41 0 5 2.2E-02 0 0
CUI: C4022987
Disease: Abnormal axonemal organization of respiratory motile cilia
Abnormal axonemal organization of respiratory motile cilia 		3 0 2 1.0E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 28 2.6E-02 0 0