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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:Saito Kuba Tsuruta Syndrome
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Accession:DOID:9001158 term browser browse the term
Synonyms:exact_synonym: Fibulo ulnar hypoplasia renal anomalies;   Fibuloulnar aplasia or hypoplasia with renal abnormalities
 primary_id: MESH:C537226
 alt_id: OMIM:228940


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Path 1
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  disease 21128
    syndrome 10833
      Saito Kuba Tsuruta Syndrome 0
Path 2
Term Annotations click to browse term
  disease 21128
    Developmental Disease 18449
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18309
        Congenital Abnormalities 7569
          Saito Kuba Tsuruta Syndrome 0
paths to the root