Search Ontology:
Human Disease

spermatogenic failure 89

Term ID
DOID:0070588
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models