Search Ontology:
Human Disease

spermatogenic failure 16

Term ID
DOID:0070184
Synonyms
  • acephalic spermatozoa syndrome
  • SPGF16
Definition
A male infertility due to acephalic spermatozoa that is characterized by autosomal recessive inheritance of acephalic spermatozoa that has_material_basis_in mutation in the SUN5 gene on chromosome 20q11. https://www.ncbi.nlm.nih.gov/pubmed/27640305
References
Ontology
Human Disease   ( DOID:0070184 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.