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Term:
glucosephosphate dehydrogenase deficiency (DOID:2862)
Annotations: Rat: (7) Mouse: (7) Human: (8) Chinchilla: (7) Bonobo: (7) Dog: (7) Squirrel: (6) Pig: (7)
Parent Terms Term With Siblings Child Terms
childhood onset GLUT1 deficiency syndrome 2  
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
congenital disorder of glycosylation +   
congenital dyserythropoietic anemia +   
Congenital Hemolytic Anemia with Emphysema and Cutis Laxa 
congenital lactase deficiency  
congenital nonspherocytic hemolytic anemia +   
congenital sucrase-isomaltase deficiency  
D-glyceric aciduria  
dehydrated hereditary stomatocytosis +   
Fructose and Galactose Intolerance 
Fructose Metabolism, Inborn Errors +   
fructose-1,6-bisphosphatase deficiency +   
fucosidosis  
galactosemia +   
Glucose-Galactose Malabsorption  
glucosephosphate dehydrogenase deficiency +   
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.
GLUT1 Deficiency Syndrome  
glycerol kinase deficiency  
glycogen metabolism disorder +   
glycoproteinosis +   
hemoglobinopathy +   
hereditary elliptocytosis +   
hereditary spherocytosis +   
hyperinsulinemic hypoglycemia +   
Hyperproglucagonemia 
intestinal disaccharidase deficiency 
Lactate Dehydrogenase Deficiency 
lactose intolerance +   
Mannosidase Deficiency Diseases +   
mucopolysaccharidosis +   
multiple carboxylase deficiency +   
Myopathy with Storage of Glycoproteins and Glycosaminoglycans 
NGLY1-deficiency  
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency  
Ogden syndrome  
overhydrated hereditary stomatocytosis  
pentosuria  
PHGDH deficiency  
Phosphoenolpyruvate Carboxykinase Deficiency +   
primary hyperoxaluria +   
pyruvate carboxylase deficiency disease +   
pyruvate decarboxylase deficiency +   
Pyruvate Metabolism, Inborn Errors +   
Red Cell Phospholipid Defect with Hemolysis 
Rh-Null Disease, Amorph Type  
Ribose 5-Phosphate Isomerase Deficiency  
sickle cell anemia +   
Stomatocytosis II  
Storage of Unusual Polysaccharide 
thalassemia +   
Transaldolase Deficiency  
Transient Erythroblastopenia of Childhood 
Trehalase Deficiency  
triosephosphate isomerase deficiency  
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to  
X-linked congenital hemolytic anemia  
Xylosidase Deficiency 
 favism  

Synonyms
Exact Synonyms: G6PD Deficiencies ;   G6PD Deficiency ;   GPD Deficiencies ;   GPD Deficiency ;   Glucose 6 Phosphate Dehydrogenase Deficiency ;   Glucose-6-Phosphate Dehydrogenase Deficiencies ;   Glucosephosphate Dehydrogenase Deficiencies ;   deficiency of G-6PD ;   deficiency of glucose 6 phosphate dehydrogenase ;   hemolytic anemia due to G6PD deficiency
Related Synonyms: G6PD IOWA ;   G6PD IOWA CITY ;   G6PD SPRINGFIELD ;   G6PD WALTER REED
Primary IDs: MESH:D005955
Alternate IDs: RDO:0002526
Xrefs: GARD:6520 ;   NCI:C98933
Definition Sources: http://en.wikipedia.org/wiki/Glucosephosphate_dehydrogenase_deficiency "DO", MESH:D005955

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