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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 35773
    Developmental Disease 28613
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 24638
        genetic disease 23830
          monogenic disease 18586
            X-linked monogenic disease 2094
              Prostate Cancer, Hereditary, X-Linked 2 0
Path 2
Term Annotations click to browse term
  disease 35773
    disease of anatomical entity 32516
      Urogenital Diseases 6481
        Urogenital Neoplasms 2920
          reproductive system neoplasm 1446
            reproductive organ cancer 1431
              male reproductive organ cancer 915
                prostate cancer 910
                  Familial Prostate Cancer 80
                    Prostate Cancer, Hereditary, X-Linked 2 0
paths to the root