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GTR Home > Conditions/Phenotypes > Spermatogenic failure 32

Spermatogenic failure 32

Summary

Spermatogenic failure-32 (SPGF32) is characterized by male infertility due to nonobstructive azoospermia. Testicular biopsy has shown absence of spermatogenic cells and a Sertoli cell-only pattern (Choi et al., 2010). For a discussion of phenotypic and genetic heterogeneity of spermatogenic failure, see 258150. [from OMIM]

Available tests

2 tests are in the database for this condition.

Clinical tests (2 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C9orf157, NOHLH, ODG5, SPATA27, SPGF32, TEB2, bA100C15.3, bHLHe80, SOHLH1
    Summary: spermatogenesis and oogenesis specific basic helix-loop-helix 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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