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Term:spermatogenic failure 12
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Accession:DOID:0070171 term browser browse the term
Definition:A male infertility characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26. (DO)
Synonyms:exact_synonym: SPGF12
 primary_id: OMIM:615413
 alt_id: DOID:9000639;   RDO:9000939
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spermatogenic failure 12 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nanos1 nanos C2HC-type zinc finger 1 JBrowse link 1 282,134,676 282,140,370 RGD:7240710

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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          spermatogenic failure 12 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 12 1
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