OBO ID: DOID:0070178 |
Term Name: | spermatogenic failure 10 | Search Ontology: | |
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Definition: | A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/22275165 | ||
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Ontology: | Human Disease ( DOID:0070178 ) |
OTHER spermatogenic failure 10 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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