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: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 1 1.9E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome 		45 0 1 1.5E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 4 1.2E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 3 3.5E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon 		20 0 2 4.9E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 4 4.3E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin 		75 0 1 1.0E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		58 0 1 1.3E-02 0 0
CUI: C4021634
Disease: Abnormality of bone marrow cell morphology
Abnormality of bone marrow cell morphology 		15 0 1 2.7E-02 0 0
CUI: C4021657
Disease: Abnormality of bone mineral density
Abnormality of bone mineral density 		22 0 1 2.3E-02 0 0
CUI: C4025692
Disease: Abnormality of calvarial morphology
Abnormality of calvarial morphology 		8 0 1 3.3E-02 0 0
CUI: C4021822
Disease: Abnormality of female external genitalia
Abnormality of female external genitalia 		15 0 1 2.7E-02 0 0
CUI: C4025900
Disease: Abnormality of female internal genitalia
Abnormality of female internal genitalia 		31 0 1 1.9E-02 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		171 0 1 5.2E-03 0 0
CUI: C4023091
Disease: Abnormality of neutrophil morphology
Abnormality of neutrophil morphology 		2 0 1 4.2E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 1 1.0E-02 0 0
CUI: C4021976
Disease: Abnormality of the lymphatic system
Abnormality of the lymphatic system 		16 0 1 2.6E-02 0 0
CUI: C4025717
Disease: Abnormality of the small intestine
Abnormality of the small intestine 		2 0 1 4.2E-02 0 0
CUI: C0267756
Disease: Abscess of peritoneum
Abscess of peritoneum 		9 0 1 3.2E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation 		111 0 1 7.5E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 1 4.4E-03 0 0
CUI: C4024848
Disease: Absent pigmentation of the ventral chest
Absent pigmentation of the ventral chest 		2 0 1 4.2E-02 0 0
CUI: C0406352
Disease: Acanthosis palmaris
Acanthosis palmaris 		4 0 1 3.8E-02 0 0
CUI: C0268603
Disease: Acetyl-CoA: carboxylase deficiency
Acetyl-CoA: carboxylase deficiency 		1 0 1 4.3E-02 0 0
CUI: C1321756
Disease: Achalasia
Achalasia 		40 0 3 5.0E-02 0 0