Search Ontology:
Human Disease
spermatogenic failure 89
- Term ID
- DOID:0070588
- Synonyms
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- SPGF89
- Definition
- A spermatogenic failure characterized by severely reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the AK9 gene on chromosome 6q21. https://pubmed.ncbi.nlm.nih.gov/37713809/
- References
- Ontology
- Human Disease ( DOID:0070588 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models