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: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		0 2 0 0 1 7.7E-02
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 8.3E-02
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder 		0 2 0 0 1 7.7E-02
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0 1 0 0 1 8.3E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 7.1E-02
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		0 2 0 0 1 7.7E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 1 0 0 1 8.3E-02
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 0.17
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 8.3E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 7.1E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 7.7E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 7.1E-02
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		0 2 0 0 1 7.7E-02
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		0 5 0 0 1 6.2E-02
CUI: C0266617
Disease: Congenital anomaly of face
Congenital anomaly of face 		106 0 1 2.4E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		104 0 1 2.4E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		68 0 1 2.6E-03 0 0
CUI: C1285498
Disease: Vegetation
Vegetation 		67 0 1 2.6E-03 0 0
CUI: C0079504
Disease: Hermanski-Pudlak Syndrome
Hermanski-Pudlak Syndrome 		63 0 1 2.6E-03 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		61 0 1 2.7E-03 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		58 0 1 2.7E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		56 0 1 2.7E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus 		51 0 1 2.7E-03 0 0
CUI: C0266463
Disease: Lissencephaly
Lissencephaly 		51 0 1 2.7E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		50 0 1 2.7E-03 0 0