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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 18203
    physical disorder 4334
      polydactyly 221
        Pseudotrisomy 13 Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18203
    Developmental Disease 13119
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11888
        genetic disease 11398
          inherited metabolic disorder 4722
            carbohydrate metabolic disorder 2591
              glucose metabolism disease 1901
                diabetes mellitus 1499
                  Diabetes Complications 483
                    Fetal Macrosomia 57
                      Pseudotrisomy 13 Syndrome 0
paths to the root