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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:XYY Karyotype
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Accession:DOID:9000426 term browser browse the term
Definition:Abnormal genetic constitution in males characterized by an extra Y chromosome.
Synonyms:exact_synonym: XYY Karyotypes
 primary_id: MESH:D014997


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47, XYY Syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
CL CVCL_8X25 HH0132 IEA NCI:C85237 CELLOSAURUS
CL CVCL_8X35 HH0299 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9C05 DD0779 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9C28 DD0808 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9D72 DD1062 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9E97 DD1287 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9F76 DD1421 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9I85 DD2111 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9I99 DD2135 IEA NCI:C85237 CELLOSAURUS
CL CVCL_9K93 DD2770 IEA NCI:C85237 CELLOSAURUS
CL CVCL_F023 GM01993 IEA NCI:C85237 CELLOSAURUS
CL CVCL_W636 GM01250 IEA NCI:C85237 CELLOSAURUS
CL CVCL_W637 GM09326 IEA NCI:C85237 CELLOSAURUS
CL CVCL_W638 GM11337 IEA NCI:C85237 CELLOSAURUS
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 29104
    Pathological Conditions, Signs and Symptoms 16597
      Pathologic Processes 10019
        Chromosome Aberrations 4269
          Abnormal Karyotype 0
            XYY Karyotype 0
              47, XYY Syndrome 0
paths to the root