Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
3-hydroxyacyl-CoA dehydrogenase deficiency pathway  
3-methylglutaconic aciduria type 1 pathway  
3-methylglutaconic aciduria type 3 pathway  
adenine phoshoribosyltransferase deficiency pathway  
AICA-ribosuria pathway  
beta-ureidopropionase deficiency pathway  
fumaric aciduria pathway  
inborn error amino acid transport disorder pathway +   
inborn error of amino acid metabolism pathway +   
inborn error of brain metabolic pathway +   
inborn error of carbohydrate metabolism pathway +   
inborn error of lipid metabolism pathway +   
inborn error of metal metabolism pathway +   
inborn error of purine-pyrimidine metabolism pathway +   
inborn error of renal tubular transport pathway +   
inborn error of steroid metabolism pathway +   
leukotriene C4 synthase deficiency pathway  
lysosomal storage disease pathway +   
malonic aciduria pathway  
A rare inherited metabolic condition due to alterations in the activity of malonyl-CoA decarboxylase.
porphyria pathway +   

Synonyms
Exact Synonyms: malonic aciduria disease pathway
Related Synonyms: SMP:00198 ;   SMP:00502 ;   malonyl-CoA decarboxylase deficiency pathway
Alternate IDs: PW:0002550
Definition Sources: OMIM:248360

paths to the root