|OBO ID: DOID:0070177|
|Term Name:||spermatogenic failure 22||Search Ontology:|
|Definition:||A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/28206990|
|Ontology:||Human Disease (DOID:0070177)|
|is a type of:||
OTHER spermatogenic failure 22 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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