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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:Trypsinogen Deficiency
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Accession:DOID:9006609 term browser browse the term
Synonyms:primary_id: MIM:614044;   RDO:9000845


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16177
    Nutritional and Metabolic Diseases 7679
      disease of metabolism 7679
        inherited metabolic disorder 6059
          Trypsinogen Deficiency 1
Path 2
Term Annotations click to browse term
  disease 16177
    Developmental Disease 13928
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 12950
        genetic disease 12639
          inherited metabolic disorder 6059
            Trypsinogen Deficiency 1
paths to the root