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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:Rudd Klimek Syndrome
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Accession:DOID:9006398 term browser browse the term
Synonyms:exact_synonym: Caudal dysgenesis familial type;   Familial caudal dysgenesis
 primary_id: MESH:C535879;   RDO:0001232


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19106
    syndrome 11278
      Rudd Klimek Syndrome 0
Path 2
Term Annotations click to browse term
  disease 19106
    Developmental Disease 14617
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13628
        Congenital Abnormalities 7782
          Musculoskeletal Abnormalities 3443
            Congenital Limb Deformities 1066
              Ectromelia 15
                Rudd Klimek Syndrome 0
paths to the root