Term:spermatogenic failure 11
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Accession:DOID:0070180 term browser browse the term
Definition:A male infertility characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. (DO)
Synonyms:exact_synonym: SPGF11
 primary_id: OMIM:615081
 alt_id: DOID:9003055;   RDO:9000819
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spermatogenic failure 11 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Klhl10 kelch-like family member 10 JBrowse link 10 88,356,652 88,372,929 RGD:7240710

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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          spermatogenic failure 11 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      Urogenital Diseases 3915
        Female Urogenital Diseases and Pregnancy Complications 1687
          Female Urogenital Diseases 1436
            female reproductive system disease 1432
              infertility 203
                male infertility 144
                  spermatogenic failure 11 1
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