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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
 alt_id: RDO:0000371
 xref: NCI:C89802
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 18145
    syndrome 9691
      49,XXXXX Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18145
    Developmental Disease 12907
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11612
        genetic disease 11118
          chromosomal disease 2328
            Sex Chromosome Disorders 51
              49,XXXXX Syndrome 0
paths to the root