Search Ontology:
Human Disease

glutaric acidemia type 3

Term ID
DOID:0112246
Synonyms
  • GA III
  • GA3
  • glutaric aciduria 3
  • glutaric aciduria III
  • glutaric aciduria type 3
  • glutaryl-CoA oxidase deficiency
Definition
A peroxisomal disease characterized by isolated accumulation of glutaric acid in the absence of other clinical phenotype that has_material_basis_in homozygous or compound heterozygous mutation in the SUGCT gene on chromosome 7p14.1. https://pubmed.ncbi.nlm.nih.gov/23893049/
References
Ontology
Human Disease   ( DOID:0112246 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models