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Pathways

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:Chromosome 9, Trisomy
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Accession:DOID:9008522 term browser browse the term
Synonyms:exact_synonym: Duplication 9;   Trisomy 9
 primary_id: MESH:C538028;   RDO:0003962
 xref: NCI:C84282



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21112
    syndrome 10710
      chromosomal duplication syndrome 1246
        Trisomy 369
          Chromosome 9, Trisomy 0
Path 2
Term Annotations click to browse term
  disease 21112
    Developmental Disease 18434
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18288
        genetic disease 18231
          chromosomal disease 2813
            chromosomal duplication syndrome 1246
              Trisomy 369
                Chromosome 9, Trisomy 0
paths to the root