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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:Pseudotrisomy 13 Syndrome
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Accession:DOID:9004419 term browser browse the term
Synonyms:exact_synonym: Pseudo trisomy 13 syndrome;   holoprosencephaly-polydactyly syndrome
 primary_id: MESH:C535829
 alt_id: OMIM:264480
 xref: NCI:C125418
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 17289
    syndrome 8166
      holoprosencephaly 72
        Pseudotrisomy 13 Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17289
    Nutritional and Metabolic Diseases 5565
      disease of metabolism 5565
        acquired metabolic disease 2898
          carbohydrate metabolism disease 1801
            glucose metabolism disease 1801
              diabetes mellitus 1407
                Diabetes Complications 415
                  Fetal Macrosomia 7
                    Pseudotrisomy 13 Syndrome 0
paths to the root