FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spermatogenic failure 22 ID (Ontology) DOID:0070177 (Human Disease)
Definition A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.
Also Known As "SPGF22"
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 Genes
 spermatogenic failure 22       1
 for disease ribbon | spermatogenic failure 22       1
 model of | spermatogenic failure 22       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
male infertility                 |
 |__spermatogenic failure________|
                                 spermatogenic failure 22  1 rec.
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Is a autosomal recessive disease
spermatogenic failure
Part of
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Synonyms
  • "SPGF22" EXACT OMO:0003012
Secondary IDs
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MIM:617706