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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

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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          spermatogenic failure 8 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      Urogenital Diseases 3755
        Female Urogenital Diseases and Pregnancy Complications 1530
          Female Urogenital Diseases 1281
            female reproductive system disease 1277
              infertility 197
                male infertility 138
                  spermatogenic failure 8 1
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