Send us a Message



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

RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:Chiari Malformation Type I with Syringomyelia
go back to main search page
Accession:DOID:9003359 term browser browse the term
Synonyms:exact_synonym: CM1 with Syringomyelia
 primary_id: MESH:C566133;   RDO:0014584
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 17126
    physical disorder 3070
      neural tube defect 119
        Arnold-Chiari Malformation 2
          Chiari Malformation Type I with Syringomyelia 0
Path 2
Term Annotations click to browse term
  disease 17126
    Developmental Disease 10894
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9430
        Congenital Abnormalities 5555
          Nervous System Malformations 1636
            neural tube defect 119
              Arnold-Chiari Malformation 2
                Chiari Malformation Type I with Syringomyelia 0
paths to the root