OBO ID: DOID:0070171 |
Term Name: | spermatogenic failure 12 | Search Ontology: | |
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Definition: | A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26. https://www.ncbi.nlm.nih.gov/pubmed/23315541 | ||
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Ontology: | Human Disease ( DOID:0070171 ) |
OTHER spermatogenic failure 12 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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