OBO ID: DOID:0110002
Term Name: 3-methylglutaconic aciduria type 1 Search Ontology:
Synonyms:
  • 3-methylglutaconic aciduria type I
  • 3-methylglutaconyl-CoA hydratase deficiency
  • 3MG-CoA hydratase deficiency
  • MGA type I
  • MGA1
Definition: A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22. https://pubmed.ncbi.nlm.nih.gov/12434311/
References:
Ontology: Human Disease   ( DOID:0110002 )
Relationships
is a type of:
OTHER 3-methylglutaconic aciduria type 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AUH 3-methylglutaconic aciduria, type I 250950
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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