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: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 1 3.2E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.0E-04 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.9E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 3.4E-02 0 0
CUI: C0001430
Disease: Adenoma
Adenoma 		1183 0 1 8.4E-04 0 0
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		577 0 1 1.7E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 1.1E-02 0 0
CUI: C0002875
Disease: Cooley's anemia
Cooley's anemia 		144 0 1 6.6E-03 0 0
CUI: C0003130
Disease: Anoxia
Anoxia 		287 0 1 3.4E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		139 0 1 6.8E-03 0 0
CUI: C0004096
Disease: Asthma
Asthma 		2096 0 1 4.8E-04 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 0 1 2.4E-02 0 0
CUI: C0004158
Disease: Athetosis
Athetosis 		39 0 1 2.2E-02 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		939 0 1 1.1E-03 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		1758 0 1 5.7E-04 0 0
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		198 0 1 4.9E-03 0 0
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		2130 0 1 4.7E-04 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		595 0 1 1.7E-03 0 0
CUI: C0005747
Disease: Blepharospasm
Blepharospasm 		44 0 1 2.0E-02 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		109 0 1 8.6E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 1.0E-02 0 0
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		1018 0 1 9.8E-04 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 0 1 1.4E-02 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		355 0 1 2.8E-03 0 0
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		757 0 1 1.3E-03 0 0