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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:Flynn Aird Syndrome
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Accession:DOID:9008101 term browser browse the term
Definition:A rare, hereditary, neurological disease that is inherited in an autosomal dominant fashion. [Wikipedia]
Synonyms:primary_id: MESH:C537066
 alt_id: OMIM:136300


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    syndrome 10886
      Flynn Aird Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18969
    Pathological Conditions, Signs and Symptoms 13342
      Signs and Symptoms 10818
        Neurologic Manifestations 10052
          sensory system disease 6960
            eye disease 3490
              retinal disease 1221
                retinal degeneration 851
                  fundus dystrophy 703
                    retinitis pigmentosa 601
                      Flynn Aird Syndrome 0
paths to the root