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fibrogenesis imperfecta ossium - Ontology Report - Rat Genome Database

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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:fibrogenesis imperfecta ossium
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Accession:DOID:0080040 term browser browse the term
Definition:A syndrome that involves abnormality of collagen synthesis in lamellar bones, with manifestations limited to the skeleton. The initial symptom is frequently spontaneous fractures. (DO)
Synonyms:exact_synonym: Baker's disease
 xref: MONDO:0000849

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Path 1
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  disease 292546
    syndrome 133709
      fibrogenesis imperfecta ossium 0
Path 2
Term Annotations click to browse term
  disease 292546
    disease of anatomical entity 276172
      musculoskeletal system disease 99812
        connective tissue disease 71902
          bone disease 52154
            Metabolic Bone Diseases 2274
              Pathologic Bone Demineralization 0
                fibrogenesis imperfecta ossium 0
paths to the root