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: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome 		15 0 1 3.4E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 2 1.7E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection 		23 0 1 2.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 2 6.3E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 1.3E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 3 3.3E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin 		75 0 1 1.1E-02 0 0
CUI: C0232769
Disease: Abnormal gallbladder function
Abnormal gallbladder function 		3 0 1 5.9E-02 0 0
CUI: C4073168
Disease: Abnormal lactate dehydrogenase activity
Abnormal lactate dehydrogenase activity 		19 0 1 3.0E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior 		19 0 1 3.0E-02 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential 		55 0 1 1.4E-02 0 0
CUI: C4025692
Disease: Abnormality of calvarial morphology
Abnormality of calvarial morphology 		8 0 1 4.5E-02 0 0
CUI: C4025350
Disease: Abnormality of glycosphingolipid metabolism
Abnormality of glycosphingolipid metabolism 		3 0 1 5.9E-02 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		171 0 3 1.6E-02 0 0
CUI: C4022810
Disease: Abnormality of nervous system morphology
Abnormality of nervous system morphology 		13 0 1 3.7E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 1 1.1E-02 0 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax 		40 0 1 1.9E-02 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 9.1E-03 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation 		111 0 1 8.0E-03 0 0
CUI: C4024848
Disease: Absent pigmentation of the ventral chest
Absent pigmentation of the ventral chest 		2 0 1 6.2E-02 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis 		22 0 1 2.8E-02 0 0
CUI: C0687751
Disease: Acanthocytosis
Acanthocytosis 		8 0 1 4.5E-02 0 0
CUI: C1321756
Disease: Achalasia
Achalasia 		40 0 1 1.9E-02 0 0
CUI: C0158458
Disease: Acquired hallux valgus
Acquired hallux valgus 		14 0 1 3.6E-02 0 0
CUI: C1135773
Disease: Acquired Metabolic Diseases, Nervous System
Acquired Metabolic Diseases, Nervous System 		2 0 1 6.2E-02 0 0