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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 male infertility 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)
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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory