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Term:spermatogenic failure 13
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Accession:DOID:0070182 term browser browse the term
Definition:A male infertility characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11. (DO)
Synonyms:exact_synonym: SPGF13
 primary_id: OMIM:615841
 alt_id: DOID:9007607;   RDO:9001058
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spermatogenic failure 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Taf4b TATA-box binding protein associated factor 4b JBrowse link 18 6,206,939 6,338,794 RGD:7240710

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Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          spermatogenic failure 13 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 13 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.