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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:Fried Goldberg Mundel Syndrome
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Accession:DOID:9005478 term browser browse the term
Synonyms:primary_id: MESH:C535640;   RDO:0000875


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18301
    syndrome 10338
      Fried Goldberg Mundel Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18301
    Developmental Disease 17912
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 17782
        Congenital Abnormalities 7605
          Musculoskeletal Abnormalities 3334
            Congenital Limb Deformities 1026
              Lower Extremity Deformities, Congenital 187
                Congenital Foot Deformities 179
                  Fried Goldberg Mundel Syndrome 0
paths to the root