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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:X Chromosome, Trisomy Xp3
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Accession:DOID:9000833 term browser browse the term
Synonyms:exact_synonym: Duplication Xp3;   Trisomy Xp3
 primary_id: MESH:C536756;   RDO:0002436

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16060
    syndrome 9207
      chromosomal duplication syndrome 1114
        Trisomy 332
          X Chromosome, Trisomy Xp3 0
Path 2
Term Annotations click to browse term
  disease 16060
    Developmental Disease 15983
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 15933
        Congenital Abnormalities 6800
          chromosomal disease 2578
            chromosomal duplication syndrome 1114
              Trisomy 332
                X Chromosome, Trisomy Xp3 0
paths to the root