|OBO ID: DOID:0070183|
|Term Name:||spermatogenic failure 5||Search 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. https://www.ncbi.nlm.nih.gov/pubmed/17435757|
|Ontology:||Human Disease (DOID:0070183)|
|is a type of:||
OTHER spermatogenic failure 5 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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