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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: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

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21118
    syndrome 10725
      Ring Chromosome 20 Syndrome 0
Path 2
Term Annotations click to browse term
  disease 21118
    Pathological Conditions, Signs and Symptoms 13262
      Pathologic Processes 7936
        Chromosome Aberrations 2498
          Ring Chromosomes 0
            Ring Chromosome 20 Syndrome 0
paths to the root