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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:Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy
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Accession:DOID:9006287 term browser browse the term
Synonyms:primary_id: MESH:C565395
 alt_id: OMIM:250450
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 20983
    Developmental Disease 18229
      bone development disease 2282
        osteochondrodysplasia 876
          Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy 0
Path 2
Term Annotations click to browse term
  disease 20983
    disease of anatomical entity 18174
      nervous system disease 14106
        peripheral nervous system disease 4077
          neuropathy 3861
            cranial nerve disease 655
              optic nerve disease 358
                optic atrophy 179
                  Hereditary Optic Atrophies 73
                    Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy 0
paths to the root