OBO ID: DOID:0070177 |
Term Name: | spermatogenic failure 22 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0070177 ) |
OTHER spermatogenic failure 22 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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