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: C0740302
Disease: 5q-syndrome
5q-syndrome 		45 0 1 1.8E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis 		38 0 2 4.1E-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 3.3E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 1.3E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME 		41 0 1 1.9E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 4 4.4E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin 		75 0 2 2.3E-02 0 0
CUI: C4025329
Disease: Abnormality of the anus
Abnormality of the anus 		16 0 1 3.6E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 1 8.3E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 9.3E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		89 0 2 2.0E-02 0 0
CUI: C1456418
Disease: Absence of muscle
Absence of muscle 		12 0 1 4.2E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation 		111 0 1 8.1E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 1 4.6E-03 0 0
CUI: C1844554
Disease: Absent fingernail
Absent fingernail 		19 0 1 3.2E-02 0 0
CUI: C1844555
Disease: Absent toenail
Absent toenail 		11 0 1 4.3E-02 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 1 1.3E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 4.5E-03 0 0
CUI: C0702166
Disease: Acne
Acne 		167 0 2 1.1E-02 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		94 0 2 1.9E-02 0 0
CUI: C0027859
Disease: Acoustic Neuroma
Acoustic Neuroma 		131 0 2 1.4E-02 0 0
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia 		64 0 2 2.7E-02 0 0
CUI: C0238120
Disease: Acquired Factor XIII Deficiency
Acquired Factor XIII Deficiency 		1 0 1 7.7E-02 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia 		89 0 2 2.0E-02 0 0