OBO ID: DOID:0070176 |
Term Name: | spermatogenic failure 4 | Search Ontology: | |
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Definition: | A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive azoospermia caused by meiotic abnormalities that has_material_basis_in mutation in the SYCP3 gene on chromosome 12q23. https://www.ncbi.nlm.nih.gov/pubmed/14643120 | ||
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Ontology: | Human Disease ( DOID:0070176 ) |
OTHER spermatogenic failure 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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