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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:Microcephaly, Retinitis Pigmentosa, and Sutural Cataract
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Accession:DOID:9006163 term browser browse the term
Synonyms:primary_id: MESH:C563296
 alt_id: MIM:601537


show annotations for term's descendants           Sort by:
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15606
    physical disorder 4906
      congenital nervous system abnormality 1497
        microcephaly 1127
          Microcephaly, Retinitis Pigmentosa, and Sutural Cataract 0
Path 2
Term Annotations click to browse term
  disease 15606
    disease of anatomical entity 15201
      nervous system disease 13269
        Neurologic Manifestations 9644
          sensory system disease 6685
            eye disease 3386
              retinal disease 1192
                retinal degeneration 838
                  fundus dystrophy 704
                    retinitis pigmentosa 603
                      Microcephaly, Retinitis Pigmentosa, and Sutural Cataract 0
paths to the root