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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:Goldstein Hutt Syndrome
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Accession:DOID:9008020 term browser browse the term
Synonyms:exact_synonym: Long eyelashes, cataract, and hereditary spherocytosis;   Trichomegaly, cataract, and hereditary spherocytosis
 primary_id: MESH:C537282;   RDO:0003096


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19102
    syndrome 11271
      Goldstein Hutt Syndrome 0
Path 2
Term Annotations click to browse term
  disease 19102
    disease of anatomical entity 18443
      Hemic and Lymphatic Diseases 4331
        hematopoietic system disease 3821
          anemia 861
            normocytic anemia 752
              hemolytic anemia 431
                congenital hemolytic anemia 364
                  hereditary spherocytosis 13
                    Goldstein Hutt Syndrome 0
paths to the root