FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spermatogenic failure 41 ID (Ontology) DOID:0111912 (Human Disease)
Definition A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2.
Also Known As "SPGF41"
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 Genes
 spermatogenic failure 41       1
 for disease ribbon | spermatogenic failure 41       1
 model of | spermatogenic failure 41       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
male infertility                 |
 |__spermatogenic failure________|
                                 spermatogenic failure 41  1 rec.
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Is a autosomal recessive disease
spermatogenic failure
Part of
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Synonyms
  • "SPGF41" EXACT OMO:0003012
Secondary IDs
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MIM:618670