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: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 5.8E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 7.4E-03 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 1.3E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.1E-03 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 1.3E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 1 5.6E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 1.2E-02 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 1.1E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 8.6E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 8.2E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 1.1E-02 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 1.4E-02 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 1.2E-02 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.4E-02 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 1.3E-02 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 1 1.3E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.3E-02 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 1.3E-02 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma 		8 0 1 1.3E-02 0 0
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion 		9 0 1 1.3E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 1.3E-02 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases 		13 0 1 1.2E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 0 1 6.3E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 1.1E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.1E-02 0 0