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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 8.3E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 8.9E-03
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		0 5 0 0 1 8.6E-03
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 1.8E-02
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 8.9E-03
CUI: C1401162
Disease: Carbohydrate intolerance
Carbohydrate intolerance 		0 1 0 0 1 8.9E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 8.9E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 8.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 8.9E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 1.8E-02
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.1E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 2.1E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 2.1E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		13 0 1 2.1E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 2.1E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.1E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 2.1E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 2.1E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 2.1E-03 2 1.8E-02
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases 		3 0 1 2.1E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 1 2.0E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 2.1E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 1.9E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.0E-03 0 0
CUI: C0002623
Disease: Post-traumatic amnesia
Post-traumatic amnesia 		9 0 1 2.1E-03 0 0