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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:Prostate Cancer, Hereditary, X-Linked 2
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Accession:DOID:9008011 term browser browse the term
Synonyms:exact_synonym: HPCX2
 primary_id: MESH:C567477
 alt_id: OMIM:300704


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16121
    Developmental Disease 13809
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 12823
        genetic disease 12470
          monogenic disease 10415
            X-linked monogenic disease 1356
              Prostate Cancer, Hereditary, X-Linked 2 0
Path 2
Term Annotations click to browse term
  disease 16121
    disease of anatomical entity 15680
      Urogenital Diseases 4907
        Urogenital Neoplasms 2194
          reproductive system neoplasm 1276
            reproductive organ cancer 1262
              male reproductive organ cancer 835
                prostate cancer 831
                  Familial Prostate Cancer 71
                    Prostate Cancer, Hereditary, X-Linked 2 0
paths to the root