DO_rare_slim has material basis in autosomal recessive disease spermatogenic failure 5 ORDO:137893 SNOMEDCT_US_2021_09_01:236806004 Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid MIM:243060 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. MESH:C562903 GARD:12385 DOID:0070183 SPGF5 disease_ontology 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 spermatogenic failure autosomal recessive inheritance