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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, 13
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Accession:DOID:9002015 term browser browse the term
Synonyms:exact_synonym: HPC13
 primary_id: MESH:C567456
 alt_id: OMIM:611928


show annotations for term's descendants           Sort by:
Prostate Cancer, Hereditary, 13 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Msmb microseminoprotein, beta ISO ClinVar Annotator: match by term: Prostate cancer, hereditary, 13
CTD Direct Evidence: marker/mechanism		 OMIM
ClinVar
CTD		 PMID:18264096 PMID:18264097 PMID:19153072 PMID:19383797 PMID:19644707 NCBI chr16:7,366,536...7,387,124
Ensembl chr16:7,366,536...7,387,123 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18976
    disease of anatomical entity 18260
      reproductive system disease 3010
        reproductive organ cancer 1266
          male reproductive organ cancer 835
            prostate cancer 831
              Familial Prostate Cancer 68
                Prostate Cancer, Hereditary, 13 1
Path 2
Term Annotations click to browse term
  disease 18976
    disease of anatomical entity 18260
      Urogenital Diseases 5234
        reproductive system disease 3010
          male reproductive system disease 2012
            Male Genital Neoplasms 1337
              Prostatic Neoplasms 1309
                prostate cancer 831
                  Familial Prostate Cancer 68
                    Prostate Cancer, Hereditary, 13 1
paths to the root