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: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		0 2 0 0 1 1.4E-02
CUI: C0009398
Disease: Color vision defect
Color vision defect 		0 4 0 0 2 2.9E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.3E-02
CUI: C0015702
Disease: Favism
Favism 		0 14 0 0 1 1.2E-02
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		0 14 0 0 2 2.5E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.5E-02
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		0 1 0 0 1 1.5E-02
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		0 5 0 0 3 4.3E-02
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		0 61 0 0 2 1.6E-02
CUI: C0152438
Disease: Sprengel deformity
Sprengel deformity 		0 4 0 0 1 1.4E-02
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration 		0 1 0 0 1 1.5E-02
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		0 5 0 0 1 1.4E-02
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		0 1 0 0 1 1.5E-02
CUI: C0242129
Disease: Thrombotic stroke
Thrombotic stroke 		0 1 0 0 1 1.5E-02
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome 		0 2 0 0 1 1.4E-02
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		0 14 0 0 4 5.1E-02
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		0 1 0 0 1 1.5E-02
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		0 6 0 0 2 2.8E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 1.5E-02
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		0 52 0 0 4 3.4E-02
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		0 1 0 0 1 1.5E-02
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		0 1 0 0 1 1.5E-02
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase 		0 63 0 0 1 7.7E-03
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 2.8E-02
CUI: C0344622
Disease: Double inlet left ventricle
Double inlet left ventricle 		0 1 0 0 1 1.5E-02