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RGD uses the Human Disease Ontology (DO, 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:Triple X Syndrome
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Accession:DOID:9007620 term browser browse the term
Synonyms:exact_synonym: 47,XXX syndrome;   47,Xxx;   Super female;   Triple-X chromosome syndrome;   Triple-X female;   Triplo X syndrome;   Trisomy X;   XXX syndrome
 primary_id: MESH:C535318;   RDO:0000369
 xref: NCI:C129718
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18110
    syndrome 9625
      Triple X Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18110
    Developmental Disease 12861
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11545
        Congenital Abnormalities 6694
          chromosomal disease 2324
            Sex Chromosome Disorders 48
              Sex Chromosome Disorders of Sex Development 15
                Triple X Syndrome 0
paths to the root