FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spermatogenic failure 39 ID (Ontology) DOID:0111926 (Human Disease)
Definition A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3.
Also Known As "SPGF39"
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 Genes
 spermatogenic failure 39       2
 for disease ribbon | spermatogenic failure 39       2
 model of | spermatogenic failure 39       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
male infertility                 |
 |__spermatogenic failure________|
                                 spermatogenic failure 39  2 rec.
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Is a autosomal recessive disease
spermatogenic failure
Part of
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Synonyms
  • "SPGF39" EXACT OMO:0003012
Secondary IDs
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MIM:618643