Search Ontology:
Human Disease

spermatogenic failure 5

Term ID
DOID:0070183
Synonyms
  • Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid
  • infertility associated with multitailed spermatozoa and excessive DNA
  • macrocephalic sperm head syndrome
  • male infertility due to macrozoospermia
  • male infertility with large-headed, multiflagellar, polyploid spermatozoa
  • SPGF5
Definition
A spermatogenic failure that is characterized by autosomal recessive inheritance of large-headed, multiflagellar, polyploid spermatozoa that has_material_basis_in mutation in the AURKC gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/17435757
References
Ontology
Human Disease   ( DOID:0070183 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models