FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spermatogenic failure 16 ID (Ontology) DOID:0070184 (Human Disease)
Definition A male infertility due to acephalic spermatozoa that is characterized by autosomal recessive inheritance of acephalic spermatozoa that has_material_basis_in mutation in the SUN5 gene on chromosome 20q11.
Also Known As "acephalic spermatozoa syndrome" ; "SPGF16"
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 Genes
 spermatogenic failure 16       2
 for disease ribbon | spermatogenic failure 16       2
 model of | spermatogenic failure 16       2
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autosomal genetic disease
 |__autosomal recessive disease____________________
spermatogenic failure                              |
 |__male infertility due to acephalic spermatozoa__|
                                                   spermatogenic failure 16  2 rec.
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Is a autosomal recessive disease
male infertility due to acephalic spermatozoa
Part of
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Synonyms
  • "acephalic spermatozoa syndrome" EXACT
    "SPGF16" EXACT OMO:0003012
Secondary IDs
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MIM:617187