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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:spermatogenic failure 14
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Accession:DOID:0070179 term browser browse the term
Definition:An azoospermia characterized by autosomal recessive inheritance of a maturation arrest in the spermatid stage of development that has_material_basis_in mutation in the ZMYND15 gene on chromosome 17p13. (DO)
Synonyms:exact_synonym: SPGF14
 primary_id: OMIM:615842
For additional species annotation, visit the Alliance of Genome Resources.


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spermatogenic failure 14 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Zmynd15 zinc finger, MYND-type containing 15 ISO OMIM NCBI chr10:57,064,482...57,071,096
Ensembl chr10:57,064,482...57,071,096
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16123
    disease of anatomical entity 15370
      reproductive system disease 2587
        male reproductive system disease 1774
          male infertility 193
            azoospermia 41
              spermatogenic failure 14 1
Path 2
Term Annotations click to browse term
  disease 16123
    disease of anatomical entity 15370
      Urogenital Diseases 4159
        Female Urogenital Diseases and Pregnancy Complications 1924
          Female Urogenital Diseases 1629
            female reproductive system disease 1625
              infertility 257
                male infertility 193
                  azoospermia 41
                    spermatogenic failure 14 1
paths to the root