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ONTOLOGY REPORT - ANNOTATIONS


Term:spermatogenic failure 8
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Accession:DOID:0070169 term browser browse the term
Definition:A male infertility characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33. (DO)
Synonyms:exact_synonym: SPGF8
 primary_id: OMIM:613957
For additional species annotation, visit the Alliance of Genome Resources.


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spermatogenic failure 8 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nr5a1 nuclear receptor subfamily 5, group A, member 1 JBrowse link 3 22,998,900 23,020,441 RGD:7240710
RGD:8554872

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Path 1
Term Annotations click to browse term
  disease 15992
    disease of anatomical entity 15263
      reproductive system disease 2485
        male reproductive system disease 1709
          male infertility 166
            spermatogenic failure 8 1
Path 2
Term Annotations click to browse term
  disease 15992
    disease of anatomical entity 15263
      Urogenital Diseases 4026
        Female Urogenital Diseases and Pregnancy Complications 1816
          Female Urogenital Diseases 1522
            female reproductive system disease 1518
              infertility 226
                male infertility 166
                  spermatogenic failure 8 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.