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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
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Accession:DOID:9003359 term browser browse the term
Synonyms:exact_synonym: CM1 with Syringomyelia
 primary_id: MESH:C566133


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 41189
    physical disorder 7135
      neural tube defect 149
        Arnold-Chiari Malformation 2
          Chiari Malformation Type I with Syringomyelia 0
Path 2
Term Annotations click to browse term
  disease 41189
    Developmental Disease 36464
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 33606
        Congenital Abnormalities 14117
          Nervous System Malformations 3148
            neural tube defect 149
              Arnold-Chiari Malformation 2
                Chiari Malformation Type I with Syringomyelia 0
paths to the root