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: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 2.3E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 3 6.4E-02 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 7.5E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		89 0 1 7.9E-03 0 0
CUI: C0426816
Disease: Absence of rib
Absence of rib 		18 0 3 5.7E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation 		111 0 1 6.8E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 2 8.3E-03 0 0
CUI: C0728895
Disease: Absent finger
Absent finger 		26 0 1 1.6E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 2.6E-02 0 0
CUI: C1405984
Disease: Absent radius
Absent radius 		24 0 1 1.6E-02 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 3.7E-03 0 0
CUI: C3276744
Disease: Absent tibia
Absent tibia 		3 0 1 2.5E-02 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 1 9.9E-03 0 0
CUI: C0266298
Disease: Accessory kidney
Accessory kidney 		20 0 1 1.8E-02 0 0
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum 		12 0 1 2.0E-02 0 0
CUI: C0345397
Disease: Accessory rib
Accessory rib 		12 0 1 2.0E-02 0 0
CUI: C0234238
Disease: Ache
Ache 		50 0 1 1.1E-02 0 0
CUI: C1860710
Disease: Achromatic retinal patches
Achromatic retinal patches 		3 0 1 2.5E-02 0 0
CUI: C0263445
Disease: Acne fulminans
Acne fulminans 		2 0 1 2.6E-02 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		120 0 2 1.3E-02 0 0
CUI: C0158486
Disease: Acquired genu recurvatum
Acquired genu recurvatum 		23 0 1 1.7E-02 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia 		89 0 1 7.9E-03 0 0
CUI: C0596032
Disease: acquired immunodeficiency
acquired immunodeficiency 		6 0 2 4.8E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 6 2.2E-02 0 0
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 1 2.4E-02 0 0