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
 alt_id: DOID:9000971;   RDO:9000816
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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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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          spermatogenic failure 8 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      Urogenital Diseases 3915
        Female Urogenital Diseases and Pregnancy Complications 1687
          Female Urogenital Diseases 1436
            female reproductive system disease 1432
              infertility 203
                male infertility 144
                  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.