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: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 0.17 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 0.17 0 0
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas 		1 0 1 0.17 0 0
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		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: C0333295
Disease: Acute ulcer
Acute ulcer 		1 0 1 0.17 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 0.17 0 0
CUI: C0523550
Disease: Catalase measurement
Catalase measurement 		1 0 1 0.17 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 0.17 0 0
CUI: C0746604
Disease: Mitral valve endocarditis
Mitral valve endocarditis 		1 0 1 0.17 0 0
CUI: C0752048
Disease: Hypocatalasemia
Hypocatalasemia 		1 0 1 0.17 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 0.17 0 0
CUI: C1171363
Disease: Renoprival hypertension
Renoprival hypertension 		1 0 1 0.17 0 0
CUI: C1291463
Disease: Deficiency of phosphoserine phosphatase
Deficiency of phosphoserine phosphatase 		1 0 1 0.17 0 0
CUI: C1536651
Disease: Arterial leg ulcer
Arterial leg ulcer 		1 0 1 0.17 0 0
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 0 1 0.17 0 0
CUI: C1849926
Disease: Phenylpyruvic acidemia
Phenylpyruvic acidemia 		1 0 1 0.17 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 0.17 0 0
CUI: C1963823
Disease: Hyperlipasaemia
Hyperlipasaemia 		1 0 1 0.17 0 0
CUI: C2363972
Disease: Histaminosis
Histaminosis 		1 0 1 0.17 0 0
CUI: C2678416
Disease: Hyperphenylalaninemia, Non-Pku Mild
Hyperphenylalaninemia, Non-Pku Mild 		1 0 1 0.17 0 0
CUI: C2936847
Disease: Acatalasemia Japanese type
Acatalasemia Japanese type 		1 0 1 0.17 0 0
CUI: C2936848
Disease: Acatalasemia Swiss type
Acatalasemia Swiss type 		1 0 1 0.17 0 0
CUI: C4016522
Disease: G6PD TOMAH PHENOTYPE
G6PD TOMAH PHENOTYPE 		1 0 1 0.17 0 0