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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:Arakawa Syndrome 2
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Accession:DOID:9000093 term browser browse the term
Synonyms:exact_synonym: Arakawa's syndrome 2;   Arakawa's syndrome II;   Methionine synthase deficiency;   N5-methylhomocysteine transferase deficiency;   Tetrahydrofolate-methyltransferase deficiency syndrome
 primary_id: MESH:C537426



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21155
    Nutritional and Metabolic Diseases 8231
      disease of metabolism 8231
        inherited metabolic disorder 6208
          amino acid metabolic disorder 1524
            Arakawa Syndrome 2 0
Path 2
Term Annotations click to browse term
  disease 21155
    Developmental Disease 18469
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18327
        genetic disease 18271
          inherited metabolic disorder 6208
            amino acid metabolic disorder 1524
              Arakawa Syndrome 2 0
paths to the root