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DO Term : 3-methylglutaconic aciduria type 1 [DOID:0110002] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22.
  • synonyms:
  • 250950,
  • 3-methylglutaconic aciduria type I,
  • OMIM:250950,
  • 3-methylglutaconyl-CoA hydratase deficiency,
  • MESH:C562801,
  • ORDO:67046,
  • 3MG-CoA hydratase deficiency,
  • MGA1,
  • MGA type I
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

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Ontology Term --> Direct parents





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