OBO ID: DOID:0112246
Term Name: glutaric acidemia type 3 Search Ontology:
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 glutaric acidemia type 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SUGCT Glutaric aciduria III 231690
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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