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Term:spermatogenic failure 14
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Accession:DOID:0070179 term browser browse the term
Definition:An azoospermia characterized by autosomal recessive inheritance of a maturation arrest in the spermatid stage of development that has_material_basis_in mutation in the ZMYND15 gene on chromosome 17p13. (DO)
Synonyms:exact_synonym: SPGF14
 primary_id: OMIM:615842
 alt_id: DOID:9001770;   RDO:9001059
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spermatogenic failure 14 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Zmynd15 zinc finger, MYND-type containing 15 JBrowse link 10 57,064,482 57,071,096 RGD:7240710

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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 14 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 14 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.