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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:Fetal Trimethadione Syndrome
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Accession:DOID:9002355 term browser browse the term
Synonyms:exact_synonym: Trimethadione embryopathy
 primary_id: MESH:C537798;   RDO:0003702
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 17445
    syndrome 8267
      Fetal Trimethadione Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17445
    Developmental Disease 11029
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9553
        Congenital Abnormalities 5651
          Abnormalities, Drug-Induced 5
            Fetal Trimethadione Syndrome 0
paths to the root