ONKI3 | Medical Subject Headings

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Glucosephosphate Dehydrogenase Deficiency

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Glucosephosphate Dehydrogenase Deficiency 19 coordinate concepts 1 subordinate concept ∟ Favism ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glucosephosphate Dehydrogenase Deficiency 19 coordinate concepts 1 subordinate concept ∟ Favism ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Glucosephosphate Dehydrogenase Deficiency 19 coordinate concepts 1 subordinate concept ∟ Favism ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glucosephosphate Dehydrogenase Deficiency 19 coordinate concepts 1 subordinate concept ∟ Favism ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Glucosephosphate Dehydrogenase Deficiency Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glucosephosphate Dehydrogenase Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Glucosephosphate Dehydrogenase Deficiency Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glucosephosphate Dehydrogenase Deficiency Anemia, Hemolytic, Congenital > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Anemia, Hemolytic, Congenital > Anemia, Hemolytic > Anemia > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Favism X
Annotation:	DF: GPD DEFIC X
historyNote*:	64 X
publicMeSHNote*:	64 X
Scope note:	A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of enzyme activity in erythrocytes, leading to hemolytic anemia. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1964-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Anemia, Dyserythropoietic, Congenital \| Anemia, Hemolytic, Congenital Nonspherocytic \| Anemia, Sickle Cell \| Elliptocytosis, Hereditary \| Hemoglobin C Disease \| Spherocytosis, Hereditary \| Thalassemia \| Carbohydrate-Deficient Glycoprotein Syndrome \| Fructose Metabolism, Inborn Errors \| Fucosidosis \| Galactosemias \| Glycogen Storage Disease \| Hyperoxaluria, Primary \| Lactose Intolerance \| Mannosidase Deficiency Diseases \| Mucolipidoses \| Mucopolysaccharidoses \| Multiple Carboxylase Deficiency \| Pyruvate Metabolism, Inborn Errors X
URI:	X
Labels and equivalent concepts:	Glukoosifosfaattidehydrogenaasin puutos (fi) GPD-puutos (fi, replaced) GPD:n puute (fi, replaced) GPD:n puutos (fi, replaced) GPD-puute (fi, replaced) Glukoosifosfaattidehydrogenaasin puute (fi, replaced) Glukosfosfatdehydrogenasbrist (sv) Deficiency, GPD (en, replaced) Glucosephosphate Dehydrogenase Deficiencies (en, replaced) GPD Deficiency (en, replaced) Deficiency, Glucosephosphate Dehydrogenase (en, replaced) X
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