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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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory