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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:Hypogonadism and Testicular Atrophy
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Accession:DOID:9000227 term browser browse the term
Synonyms:narrow_synonym: TESTICULAR ATROPHY
 primary_id: MESH:C567108


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Hypogonadism and Testicular Atrophy term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 ISO ClinVar Annotator: match by term: Testicular atrophy ClinVar PMID:25741868 PMID:26392352 PMID:28492532 NCBI chr 4:152,156,890...152,199,855
Ensembl chr 4:152,156,955...152,199,857 		JBrowse link
G Slc30a7 solute carrier family 30 (zinc transporter), member 7 ISO ClinVar Annotator: match by term: Testicular atrophy ClinVar PMID:25741868 PMID:36821639 NCBI chr 3:115,732,622...115,801,079
Ensembl chr 3:115,732,622...115,801,055 		JBrowse link
G Trp53 transformation related protein 53 ISO RGD PMID:28834365 RGD:14995504 NCBI chr11:69,471,174...69,482,699
Ensembl chr11:69,471,185...69,482,699 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18301
    disease of anatomical entity 15631
      endocrine system disease 6290
        gonadal disease 1219
          hypogonadism 209
            Hypogonadism and Testicular Atrophy 3
paths to the root