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Chinchilla Research Resource Database


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 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          spermatogenic failure 11 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      Urogenital Diseases 3755
        Female Urogenital Diseases and Pregnancy Complications 1530
          Female Urogenital Diseases 1281
            female reproductive system disease 1277
              infertility 197
                male infertility 138
                  spermatogenic failure 11 1
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