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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:Oculodentodigital Dysplasia, Autosomal Recessive
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Accession:DOID:9004641 term browser browse the term
Synonyms:exact_synonym: ODDD, autosomal recessive;   ODOD, autosomal recessive;   oculodentodigital dysplasia, autosomal recessive;   oculodentoosseous dysplasia, autosomal recessive;   oculodentoosseous dysplasia, recessive
 primary_id: MESH:C567605
 alt_id: MESH:C537733;   MIM:257850


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15426
    syndrome 10415
      oculodentodigital dysplasia 2
        Oculodentodigital Dysplasia, Autosomal Recessive 2
Path 2
Term Annotations click to browse term
  disease 15426
    disease of anatomical entity 15095
      musculoskeletal system disease 7846
        connective tissue disease 5376
          bone disease 3869
            bone development disease 2326
              dysostosis 617
                synostosis 389
                  syndactyly 146
                    oculodentodigital dysplasia 2
                      Oculodentodigital Dysplasia, Autosomal Recessive 2
paths to the root