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: C0019054
Disease: Hemolysis (disorder)
Hemolysis (disorder) 		6 0 6 1.00 0 0
CUI: C0341047
Disease: Hypertrophy of parotid gland
Hypertrophy of parotid gland 		7 0 2 0.18 0 0
CUI: C0016479
Disease: Food Poisoning
Food Poisoning 		1 0 1 0.17 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 0.17 0 0
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		36 0 6 0.17 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome 		1 0 1 0.17 0 0
CUI: C0264134
Disease: Hallux Rigidus
Hallux Rigidus 		1 0 1 0.17 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 0.17 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 0.17 0 0
CUI: C0276876
Disease: Infection by Leishmania infantum
Infection by Leishmania infantum 		1 0 1 0.17 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 0.17 0 0
CUI: C0391860
Disease: Diffuse inflammation
Diffuse inflammation 		1 0 1 0.17 0 0
CUI: C0518959
Disease: Left atrial myxoma
Left atrial myxoma 		1 0 1 0.17 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 0.17 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease 		1 0 1 0.17 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 0.17 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 0.17 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 0.17 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 0.17 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 0.17 0 0
CUI: C2350449
Disease: Pancreatitis, Graft
Pancreatitis, Graft 		1 0 1 0.17 0 0
CUI: C4016522
Disease: G6PD TOMAH PHENOTYPE
G6PD TOMAH PHENOTYPE 		1 0 1 0.17 0 0
CUI: C4302087
Disease: Silent cerebral infarct
Silent cerebral infarct 		1 0 1 0.17 0 0
CUI: C4317046
Disease: Hematological abnormality
Hematological abnormality 		1 0 1 0.17 0 0
CUI: C4509818
Disease: Facial onset sensory and motor neuronopathy syndrome
Facial onset sensory and motor neuronopathy syndrome 		1 0 1 0.17 0 0