About   Help   FAQ
Disease Ontology Browser
spermatogenic failure 5 (DOID:0070183)
Alliance: disease page
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
Alt IDs: OMIM:243060, MESH:C562903, ORDO:137893
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
02/27/2024
MGI 6.23
The Jackson Laboratory