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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

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21086
    syndrome 10782
      Triple X Syndrome 0
Path 2
Term Annotations click to browse term
  disease 21086
    Developmental Disease 18380
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18236
        Congenital Abnormalities 7501
          chromosomal disease 2824
            Sex Chromosome Disorders 70
              Sex Chromosome Disorders of Sex Development 25
                Triple X Syndrome 0
paths to the root