G6PD, glucose-6-phosphate dehydrogenase, 2539

N. diseases: 410; N. variants: 66
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 0.020 None 1.000 2 1977 2002
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Congenital Abnormality 1 0.020 None 1.000 2 1988 1992
CUI: C0152072
Disease: Ovale malaria
Ovale malaria
disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0746365
Disease: malaria relapse
malaria relapse
disease Disease or Syndrome 1 0.010 None < 0.001 1 2016 2016
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 1 0.010 None 1.000 1 2011 2011
6-Phosphogluconolactonase Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 1985 1985
CUI: C4302087
Disease: Silent cerebral infarct
Silent cerebral infarct
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2012 2012
CUI: C4317046
Disease: Hematological abnormality
Hematological abnormality
disease Disease or Syndrome 1 4 0.010 None < 0.001 1 1977 1977
CUI: C4016522
Disease: G6PD TOMAH PHENOTYPE
G6PD TOMAH PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
Chronic non-spherocytic hemolytic anemia
disease Disease or Syndrome 2 4 0.080 None 0.875 8 2 1980 2011
CUI: C0271930
Disease: Anemia of pregnancy
Anemia of pregnancy
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1991 1991
Uridine monophosphate hydrolase deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1982 1982
CUI: C0398563
Disease: Deficiency of hexokinase (disorder)
Deficiency of hexokinase (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 1986 1986
CUI: C0857812
Disease: Sickle cell-beta^+^-thalassemia
Sickle cell-beta^+^-thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
Deficiency of glucose-6-phosphate isomerase
disease Disease or Syndrome 2 0.010 None 1.000 1 2004 2004
Deficiency of bisphosphoglycerate mutase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 3 0.010 None 1.000 1 2004 2004
CUI: C4020827
Disease: Neonatal hemolytic anemia
Neonatal hemolytic anemia
disease Disease or Syndrome 2 1 0.010 None 1.000 1 2004 2004
CUI: C4021648
Disease: Fava bean-induced hemolytic anemia
Fava bean-induced hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.100 None 0
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 54 0.700 strong 1.000 115 53 1969 2019
CUI: C1387528
Disease: Acute haemolytic anaemia
Acute haemolytic anaemia
disease Disease or Syndrome 3 0.100 None 1.000 13 1984 2019
CUI: C0242183
Disease: Jaundice, Hemolytic
Jaundice, Hemolytic
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 3 0.020 None 1.000 2 1984 2019
CUI: C0272082
Disease: Hemoglobin E trait
Hemoglobin E trait
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.020 None 1.000 2 1995 2016
CUI: C0272105
Disease: Anemia due to infection
Anemia due to infection
disease Pathological Conditions, Signs and Symptoms; Infections; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2003 2003
CUI: C2242796
Disease: Sickle cell-thalassemia disease
Sickle cell-thalassemia disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 4 0.020 None 1.000 2 1985 1991