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Term:spermatogenic failure 22
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Accession:DOID:0070177 term browser browse the term
Definition:An azoospermia characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13. (DO)
Synonyms:exact_synonym: SPGF22
 primary_id: OMIM:617706
 alt_id: DOID:9001279;   RDO:9005201
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spermatogenic failure 22 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Meiob meiosis specific with OB-fold JBrowse link 10 14,174,645 14,206,026 RGD:8554872

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Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          spermatogenic failure 22 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
                  azoospermia 24
                    spermatogenic failure 22 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.