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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:Defect in Hydroxylation of Diphenylhydantoin
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Accession:DOID:9003761 term browser browse the term
Synonyms:primary_id: MESH:C565044


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19138
    Nutritional and Metabolic Diseases 8548
      disease of metabolism 8548
        inherited metabolic disorder 6626
          Defect in Hydroxylation of Diphenylhydantoin 0
Path 2
Term Annotations click to browse term
  disease 19138
    Developmental Disease 14663
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13713
        genetic disease 13378
          inherited metabolic disorder 6626
            Defect in Hydroxylation of Diphenylhydantoin 0
paths to the root