Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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:X-Linked Spermatogenic Failure 4
go back to main search page
Accession:DOID:9001624 term browser browse the term
Definition:Characterized by male infertility due to azoospermia or oligoasthenoteratozoospermia. Caused by hemizygous mutation in the GCNA gene on chromosome Xq13.
Synonyms:exact_synonym: SPGFX4
 primary_id: OMIM:301077



show annotations for term's descendants           Sort by:

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21142
    disease of anatomical entity 18190
      reproductive system disease 2980
        male reproductive system disease 1976
          male infertility 266
            spermatogenic failure 131
              X-Linked Spermatogenic Failure 4 0
Path 2
Term Annotations click to browse term
  disease 21142
    disease of anatomical entity 18190
      Urogenital Diseases 5187
        Female Urogenital Diseases and Pregnancy Complications 2419
          Female Urogenital Diseases 1971
            female reproductive system disease 1968
              infertility 357
                male infertility 266
                  spermatogenic failure 131
                    X-Linked Spermatogenic Failure 4 0
paths to the root