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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: 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
RGD:8554872

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Path 1
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  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          spermatogenic failure 12 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      Urogenital Diseases 3916
        Female Urogenital Diseases and Pregnancy Complications 1699
          Female Urogenital Diseases 1447
            female reproductive system disease 1443
              infertility 205
                male infertility 146
                  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.