Search Ontology:
Human Disease

spermatogenic failure 78

Term ID
DOID:0070577
Synonyms
  • SPGF78
Definition
A spermatogenic failure characterized by sperm with abnormal acrosome structure due to a manchette assembly defect that has_material_basis_in homozygous mutation in the IQCN gene on chromosome 19p13.11. https://pubmed.ncbi.nlm.nih.gov/36321563/
References
Ontology
Human Disease   ( DOID:0070577 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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