propionic acidemia

Summary
Synonym
  • GLYCINEMIA, KETOTIC
  • KETOTIC HYPERGLYCINEMIA
  • ketotic II glycinemia
  • ketotic glycinemia
  • propionic aciduria
  • propionyl-CoA carboxylase deficiency
Definition
An organic acidemia that involes a nonfunctional propionyl CoA carboxylase affecting conversion of amino acids and fats into sugar for energy.
Super Class
organic acidemia
External Links
Disease Ontology
DOID:14701
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
2878 GPX3 glutathione peroxidase 3
4594 MMUT methylmalonyl-CoA mutase
4968 OGG1 8-oxoguanine DNA glycosylase
5095 PCCA propionyl-CoA carboxylase subunit alpha
5096 PCCB propionyl-CoA carboxylase subunit beta
The Human Phenotype Ontology
Displaying entries 31 - 40 of 40 in total
HPO ID HPO Term
HP:0002509 Limb hypertonia
HP:0002789 Tachypnea
HP:0003108 Hyperglycinuria
HP:0003128 Lactic acidosis
HP:0004322 Short stature
HP:0004396 Poor appetite
HP:0006846 Acute encephalopathy
HP:0008872 Feeding difficulties in infancy
HP:0008936 Axial hypotonia
HP:0011695 Cerebellar hemorrhage
Displaying all 2 entries
Gene ID Gene Symbol Description
5095 PCCA propionyl-CoA carboxylase subunit alpha
5096 PCCB propionyl-CoA carboxylase subunit beta

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024