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Ontology Browser

Term:
D-glycericacidemia pathway (PW:0002212)
Annotations: Rat: (13) Mouse: (13) Human: (13) Chinchilla: (12) Bonobo: (12) Dog: (13) Squirrel: (13) Pig: (13)
Parent Terms Term With Siblings Child Terms
congenital sucrase-isomaltase deficiency pathway  
D-glycericacidemia pathway  
A very rare autosomal recessive condition resulting from alterations in glycerolipid metabolism due to defects in the glycerate kinase (GLYCTK) gene.
galactosemias pathway +   
Glut1 deficiency syndrome pathway  
glycerol kinase deficiency pathway  
glycogen storage disease pathway +   
inborn error of fructose metabolism pathway +   
inborn error of pyruvate metabolism pathway +   
mucopolysaccharidoses pathway 
multiple carboxylase deficiency pathway +   
phosphoenolpyruvate carboxykinase deficiency pathway  
primary hyperoxaluria pathway +   
ribose 5-phosphate isomerase deficiency pathway  
transaldolase deficiency pathway  
triosephosphate isomerase deficiency pathway  

Synonyms
Exact Synonyms: D-glycericacidemia disease pathway
Related Synonyms: D-glyceric aciduria disease pathway ;   SMP:00529
Definition Sources: OMIM:220120

paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.