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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:Alport Syndrome-Like Hereditary Nephritis
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Accession:DOID:9008139 term browser browse the term
Synonyms:primary_id: MESH:C562890;   RDO:0012416


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    syndrome 10832
      Alport syndrome 17
        Alport Syndrome-Like Hereditary Nephritis 0
Path 2
Term Annotations click to browse term
  disease 21128
    disease of anatomical entity 18212
      Urogenital Diseases 5216
        urinary system disease 2823
          kidney disease 2579
            nephritis 484
              Alport syndrome 17
                Alport Syndrome-Like Hereditary Nephritis 0
paths to the root