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: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		23 0 2 4.3E-02 0 0
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia 		24 13 2 4.2E-02 1 2.1E-02
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		25 0 2 4.1E-02 0 0
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
Iron-Refractory Iron Deficiency Anemia 		51 0 3 4.1E-02 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia 		26 4 2 4.0E-02 2 5.3E-02
CUI: C0007862
Disease: Cervico-Brachial Neuralgia
Cervico-Brachial Neuralgia 		1 0 1 3.8E-02 0 0
CUI: C0085920
Disease: Brachial Neuralgia
Brachial Neuralgia 		1 0 1 3.8E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 3.8E-02 0 0
CUI: C0241850
Disease: COORDINATION DEFICIT
COORDINATION DEFICIT 		1 0 1 3.8E-02 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 3.8E-02 1 2.8E-02
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 3.8E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 3.8E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 3.8E-02 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 3.8E-02 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 3.8E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 3.8E-02 0 0
CUI: C1837229
Disease: Muscular Dystrophy, Congenital, Type 1D
Muscular Dystrophy, Congenital, Type 1D 		1 0 1 3.8E-02 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 3.8E-02 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 3.8E-02 1 2.8E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 3.8E-02 1 2.8E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 3.8E-02 2 5.6E-02
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital 		1 0 1 3.8E-02 0 0
CUI: C2675491
Disease: AMYOTROPHIC LATERAL SCLEROSIS 11
AMYOTROPHIC LATERAL SCLEROSIS 11 		1 0 1 3.8E-02 0 0
CUI: C3150414
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 		1 0 1 3.8E-02 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 3.8E-02 1 2.8E-02