Search Ontology:
Human Disease
spermatogenic failure 39
- Term ID
- DOID:0111926
- Synonyms
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- 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. https://pubmed.ncbi.nlm.nih.gov/31178125/
- References
- Ontology
- Human Disease ( DOID:0111926 )
- is a type of
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Genes Involved
Zebrafish Models