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ONTOLOGY REPORT - ANNOTATIONS


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: 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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Path 1
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      reproductive system disease 2487
        male reproductive system disease 1710
          male infertility 167
            spermatogenic failure 12 1
Path 2
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      Urogenital Diseases 4027
        Female Urogenital Diseases and Pregnancy Complications 1817
          Female Urogenital Diseases 1523
            female reproductive system disease 1519
              infertility 227
                male infertility 167
                  spermatogenic failure 12 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.