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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:49,XXXXX Syndrome
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Accession:DOID:9000979 term browser browse the term
Synonyms:exact_synonym: Chromosome X pentasomy;   Chromosome XXXXX syndrome;   Penta-X syndrome;   Pentasomy X;   Pentasomy X syndrome
 primary_id: MESH:C535319
 xref: NCI:C89802

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21118
    syndrome 10725
      49,XXXXX Syndrome 0
Path 2
Term Annotations click to browse term
  disease 21118
    Developmental Disease 18449
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18310
        genetic disease 18254
          chromosomal disease 2688
            Sex Chromosome Disorders 68
              49,XXXXX Syndrome 0
paths to the root