| Term Name: | spermatogenic failure 39 |
|---|---|
| Synonyms: | SPGF39 |
| 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. |
| Ontology: | Human Disease [DOID:0111926] ( DOID:0111926 ) |