FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spermatogenic failure 10 ID (Ontology) DOID:0070178 (Human Disease)
Definition A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13.
Also Known As "Spermatogenic failure with defective sperm annulus" ; "SPGF10"
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 Genes
 spermatogenic failure 10       1
 for disease ribbon | spermatogenic failure 10       1
 model of | spermatogenic failure 10       1
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autosomal genetic disease
 |__autosomal dominant disease__
male infertility                |
 |__spermatogenic failure_______|
                                spermatogenic failure 10  1 rec.
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Is a autosomal dominant disease
spermatogenic failure
Part of
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Synonyms
  • "Spermatogenic failure with defective sperm annulus" EXACT
    "SPGF10" EXACT OMO:0003012
Secondary IDs
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MIM:614822