Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   


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:Warfarin Syndrome
go back to main search page
Accession:DOID:9004297 term browser browse the term
Synonyms:exact_synonym: Congenital warfarin syndrome;   Coumarin syndrome;   DiSala syndrome;   Fetal anticoagulant syndrome;   Warfarin embryopathy
 primary_id: MESH:C536683;   RDO:0002328
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17445
    syndrome 8267
      Warfarin 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
            Warfarin Syndrome 0
paths to the root