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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 16023
    syndrome 7003
      holoprosencephaly 36
        Pseudotrisomy 13 Syndrome 0
Path 2
Term Annotations click to browse term
  disease 16023
    Nutritional and Metabolic Diseases 4727
      disease of metabolism 4727
        acquired metabolic disease 2786
          carbohydrate metabolism disease 1757
            glucose metabolism disease 1757
              diabetes mellitus 1371
                Diabetes Complications 405
                  Fetal Macrosomia 7
                    Pseudotrisomy 13 Syndrome 0
paths to the root


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