Search Ontology:
Human Disease

3-methylglutaconic aciduria type 1

Term ID
DOID:0110002
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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