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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 16269
    syndrome 10876
      oculodentodigital dysplasia 2
        Oculodentodigital Dysplasia, Autosomal Recessive 2
Path 2
Term Annotations click to browse term
  disease 16269
    disease of anatomical entity 15860
      musculoskeletal system disease 8124
        connective tissue disease 5551
          bone disease 3991
            bone development disease 2377
              dysostosis 637
                synostosis 403
                  syndactyly 150
                    oculodentodigital dysplasia 2
                      Oculodentodigital Dysplasia, Autosomal Recessive 2
paths to the root