Concept information
- Fields of Study
- diseases and disorders (animals and humans)
- noninfectious diseases
- genetic disorders
- inherited metabolic diseases
- Animals, Livestock, One Health
- diseases and disorders (animals and humans)
- noninfectious diseases
- genetic disorders
- inherited metabolic diseases
- Fields of Study
- diseases and disorders (animal and human)
- noninfectious diseases
- genetic disorders
- inherited metabolic diseases
- Research, Technology, Methods
- diseases and disorders (animal and human)
- noninfectious diseases
- genetic disorders
- inherited metabolic diseases
- Research, Technology, Methods
- diseases and disorders (animal and human)
- noninfectious diseases
- genetic disorders
- inherited metabolic diseases
- Fields of Study
- diseases and disorders (animals and humans)
- noninfectious diseases
- metabolic diseases
- inherited metabolic diseases
- Animals, Livestock, One Health
- diseases and disorders (animals and humans)
- noninfectious diseases
- metabolic diseases
- inherited metabolic diseases
- Fields of Study
- diseases and disorders (animal and human)
- noninfectious diseases
- metabolic diseases
- inherited metabolic diseases
- Research, Technology, Methods
- diseases and disorders (animal and human)
- noninfectious diseases
- metabolic diseases
- inherited metabolic diseases
- Research, Technology, Methods
- diseases and disorders (animal and human)
- noninfectious diseases
- metabolic diseases
- inherited metabolic diseases
Término preferido
glucosephosphate dehydrogenase deficiency
Tipo
-
Topic
Definición
-
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.
Fuente: Medical Subject Headings 2015
Tipo: Concept definition
Concepto genérico
Conceptos específicos
Sinónimos
- G6PD deficiency
En otras lenguas
URI
https://lod.nal.usda.gov/nalt/245231
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