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.
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: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
disease Hemic and Lymphatic Diseases Disease or Syndrome 154 31 0.600 strong 1.000 47 2 1973 2019
CUI: C0015702
Disease: Favism
Favism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Chemically-Induced Disorders; Hemic and Lymphatic Diseases Disease or Syndrome 11 14 0.600 None 1.000 26 6 1971 2018
Deficiency of glucose-6-phosphate dehydrogenase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 75 20 0.500 None 0.970 199 16 1971 2020
CUI: C0024530
Disease: Malaria
Malaria
disease Infections Disease or Syndrome 685 148 0.400 None 0.952 84 1978 2020
CUI: C0520572
Disease: Enzymopathy
Enzymopathy
group Nutritional and Metabolic Diseases Disease or Syndrome 17 1 0.400 strong 1.000 33 1990 2018
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group Neoplasms Neoplastic Process 8621 1641 0.400 None 0.875 16 2 1977 2019
Anemia, Hemolytic, Congenital Nonspherocytic
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 0.400 None 1.000 15 1973 2017
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 1183 839 0.330 None 1.000 7 1981 2019
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 826 32 0.320 None 0.800 5 1973 2019
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 36 0.310 None 1.000 3 1970 2019
Granulomatous Disease, Chronic, X-Linked
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 75 0.310 None 1.000 2 1973 1994
CUI: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 491 0.310 strong 1.000 2 1987 2002
CUI: C0018203
Disease: Chronic granulomatous disease
Chronic granulomatous disease
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 105 23 0.310 None 1.000 2 1973 1994
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 31 0.300 None 1.000 3 1973 1996
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning 185 3 0.300 None 1.000 3 1973 1978
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic
disease Hemic and Lymphatic Diseases Disease or Syndrome 13 0.300 None 1.000 3 1973 1996
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired
disease Hemic and Lymphatic Diseases Disease or Syndrome 16 1 0.300 None 1.000 3 1973 1996
CUI: C1565662
Disease: Acute Kidney Insufficiency
Acute Kidney Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 104 0.300 None 1.000 3 1973 1978
CUI: C0312854
Disease: Extravascular Hemolysis
Extravascular Hemolysis
disease Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 2 1970 1978
CUI: C0019054
Disease: Hemolysis (disorder)
Hemolysis (disorder)
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 2 1970 1978
CUI: C0031306
Disease: Phagocyte Bactericidal Dysfunction
Phagocyte Bactericidal Dysfunction
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.300 None 1.000 1 1973 1973
Autosomal Recessive Chronic Granulomatous Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.300 None 1.000 1 1973 1973
CUI: C0162351
Disease: Contact hypersensitivity
Contact hypersensitivity
phenotype Skin and Connective Tissue Diseases Pathologic Function 71 0.300 None 1.000 1 2015 2015
CUI: C0011616
Disease: Contact Dermatitis
Contact Dermatitis
disease Skin and Connective Tissue Diseases Disease or Syndrome 110 3 0.300 None 1.000 1 2015 2015