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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:3-methylglutaconic aciduria type 4
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Accession:DOID:0110006 term browser browse the term
Definition:A 3-methylglutaconic aciduria that is characterized by mild or intermittent urinary excretion of 3-methylglutaconic acid. (DO)
Synonyms:exact_synonym: 3-methylglutaconic aciduria type IV;   MGA Type IV;   MGA4;   MGCA4
 primary_id: MESH:C565393
 alt_id: OMIM:250951;   RDO:0014040
 xref: ORDO:67048


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    Nutritional and Metabolic Diseases 8235
      disease of metabolism 8235
        inherited metabolic disorder 6212
          3-methylglutaconic aciduria 152
            3-methylglutaconic aciduria type 4 0
Path 2
Term Annotations click to browse term
  disease 21128
    Developmental Disease 18448
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18308
        genetic disease 18252
          inherited metabolic disorder 6212
            amino acid metabolic disorder 1525
              organic acidemia 384
                3-methylglutaconic aciduria 152
                  3-methylglutaconic aciduria type 4 0
paths to the root