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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 1.9E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 1 0 0 1 1.9E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.9E-02
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0 1 0 0 1 1.9E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		0 2 0 0 1 1.8E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 1.8E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 1.9E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 1.8E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 1 0 0 1 1.9E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 1.8E-02
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		0 1 0 0 1 1.9E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 1.8E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 1.8E-02
CUI: C2939175
Disease: Meconium ileus
Meconium ileus 		0 11 0 0 1 1.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.9E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.9E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 1.6E-02
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		0 5 0 0 1 1.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.8E-02
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		57 0 1 1.5E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		45 0 1 1.6E-03 0 0
CUI: C0024591
Disease: Malignant hyperpyrexia due to anesthesia
Malignant hyperpyrexia due to anesthesia 		39 0 1 1.6E-03 0 0
CUI: C0270972
Disease: Cornelia De Lange Syndrome
Cornelia De Lange Syndrome 		38 0 1 1.6E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		38 0 1 1.6E-03 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		34 0 1 1.6E-03 0 0