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RGD uses the Human Disease Ontology (DO, 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 6
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Accession:DOID:0070167 term browser browse the term
Definition:A male infertility characterized by autosomal recessive inheritance of globozoospermia that has_material_basis_in mutation in the SPATA16 gene on chromosome 3q26. (DO)
Synonyms:exact_synonym: SPGF6;   acrosome malformation of spermatozoa;   round-headed spermatozoa
 broad_synonym: globozoospermia
 primary_id: OMIM:102530
For additional species annotation, visit the Alliance of Genome Resources.

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spermatogenic failure 6 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Spata16 spermatogenesis associated 16 ISO OMIM NCBI chr 2:112,281,326...112,659,911
Ensembl chr 2:112,281,376...112,659,927
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16091
    disease of anatomical entity 15341
      reproductive system disease 2573
        male reproductive system disease 1763
          male infertility 183
            spermatogenic failure 70
              spermatogenic failure 6 1
Path 2
Term Annotations click to browse term
  disease 16091
    disease of anatomical entity 15341
      Urogenital Diseases 4146
        Female Urogenital Diseases and Pregnancy Complications 1913
          Female Urogenital Diseases 1619
            female reproductive system disease 1615
              infertility 247
                male infertility 183
                  Teratozoospermia 7
                    Globozoospermia 2
                      spermatogenic failure 6 1
paths to the root