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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:Y-linked spermatogenic failure 1
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Accession:DOID:0070186 term browser browse the term
Definition:A Sertoli cell-only syndrome that has_material_basis_in deletions in the Yq11 chromosomal region. (DO)
Synonyms:exact_synonym: SPGFY1;   Sertoli cell-only syndrome, Y-linked;   Sertoli cell-only syndrome, type 1;   Sertoli cell-only syndrome, type I
 narrow_synonym: INCOMPLETE SERTOLI CELL-ONLY SYNDROME;   hypospermatogenesis
 primary_id: MESH:C537587
 alt_id: OMIM:400042
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16023
    syndrome 7003
      Sertoli cell-only syndrome 3
        Y-linked spermatogenic failure 1 0
Path 2
Term Annotations click to browse term
  disease 16023
    disease of anatomical entity 15278
      Urogenital Diseases 4155
        Female Urogenital Diseases and Pregnancy Complications 1915
          Female Urogenital Diseases 1612
            female reproductive system disease 1608
              infertility 240
                male infertility 177
                  Sertoli cell-only syndrome 3
                    Y-linked spermatogenic failure 1 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.