Source: BEFREE ×
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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 4.1E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 4.0E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 4.1E-03
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		0 2 0 0 1 4.0E-03
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 1 0 0 1 4.1E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 4.1E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 4.0E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 4.0E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 4.0E-03
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 4.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 4.0E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.1E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 4.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 8.1E-03
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis 		2 0 1 4.0E-04 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 4.0E-04 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 4.0E-04 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil 		2 0 1 4.0E-04 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		8 0 1 4.0E-04 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 4.0E-04 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 4.0E-04 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		6 0 1 4.0E-04 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		1 0 1 4.0E-04 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity 		1 0 1 4.0E-04 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		3 0 1 4.0E-04 0 0