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Summary Literature (0)
DOID:0070183 - spermatogenic failure 5

Disease Ontology 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.

Synonyms: Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid, SPGF5, 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,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009461 - spermatogenic failure 5


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), male infertility (is_a), spermatogenic failure (is_a)