OBO ID: DOID:0070180 |
Term Name: | spermatogenic failure 11 | Search Ontology: | |
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Definition: | A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/17047026 | ||
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Ontology: | Human Disease ( DOID:0070180 ) |
OTHER spermatogenic failure 11 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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