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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:Ring Chromosome 20 Syndrome
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Accession:DOID:9002466 term browser browse the term
Synonyms:exact_synonym: R(20) Syndrome;   Ring 20 Syndrome;   Ring Chromosome 20;   Ring Chromosome 20 Epilepsy Syndrome
 primary_id: MESH:C535369;   MESH:C580424;   RDO:0015922
 alt_id: RDO:0000451
 xref: NCI:C169001
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 16023
    syndrome 7003
      Ring Chromosome 20 Syndrome 0
Path 2
Term Annotations click to browse term
  disease 16023
    Pathological Conditions, Signs and Symptoms 8754
      Pathologic Processes 6130
        Chromosome Aberrations 1723
          Ring Chromosomes 0
            Ring Chromosome 20 Syndrome 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.