Glucosephosphate Dehydrogenase Deficiency
"Glucosephosphate Dehydrogenase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.
Descriptor ID |
D005955
|
MeSH Number(s) |
C15.378.071.141.150.480 C16.320.070.480 C16.320.565.202.402 C18.452.648.202.402
|
Concept/Terms |
Glucosephosphate Dehydrogenase Deficiency- Glucosephosphate Dehydrogenase Deficiency
- Deficiencies, Glucosephosphate Dehydrogenase
- Dehydrogenase Deficiencies, Glucosephosphate
- Dehydrogenase Deficiency, Glucosephosphate
- Deficiency, GPD
- Deficiencies, GPD
- GPD Deficiencies
- G6PD Deficiency
- Deficiencies, G6PD
- Deficiency, G6PD
- G6PD Deficiencies
- Glucose 6 Phosphate Dehydrogenase Deficiency
- Glucosephosphate Dehydrogenase Deficiencies
- GPD Deficiency
- Hemolytic Anemia Due to G6PD Deficiency
- Deficiency of Glucose-6-Phosphate Dehydrogenase
- Deficiency of Glucose 6 Phosphate Dehydrogenase
- Deficiency, Glucosephosphate Dehydrogenase
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Deficiencies, Glucose-6-Phosphate Dehydrogenase
- Deficiency, Glucose-6-Phosphate Dehydrogenase
- Dehydrogenase Deficiencies, Glucose-6-Phosphate
- Dehydrogenase Deficiency, Glucose-6-Phosphate
- Glucose-6-Phosphate Dehydrogenase Deficiencies
|
Below are MeSH descriptors whose meaning is more general than "Glucosephosphate Dehydrogenase Deficiency".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Glucosephosphate Dehydrogenase Deficiency [C15.378.071.141.150.480]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Glucosephosphate Dehydrogenase Deficiency [C16.320.070.480]
- Metabolism, Inborn Errors [C16.320.565]
- Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
- Glucosephosphate Dehydrogenase Deficiency [C16.320.565.202.402]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
- Glucosephosphate Dehydrogenase Deficiency [C18.452.648.202.402]
Below are MeSH descriptors whose meaning is more specific than "Glucosephosphate Dehydrogenase Deficiency".
- Glucosephosphate Dehydrogenase Deficiency
- Favism
This graph shows the total number of publications written about "Glucosephosphate Dehydrogenase Deficiency" by people in this website by year, and whether "Glucosephosphate Dehydrogenase Deficiency" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2014 | 0 | 1 | 1 |
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Below are the most recent publications written about "Glucosephosphate Dehydrogenase Deficiency" by people in Profiles.
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Incidence, etiology, and outcomes of hazardous hyperbilirubinemia in newborns. Pediatrics. 2014 Sep; 134(3):504-9.