OBO ID: DOID:0070169 |
Term Name: | spermatogenic failure 8 | Search Ontology: | |
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Definition: | A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/20887963 | ||
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Ontology: | Human Disease ( DOID:0070169 ) |
OTHER spermatogenic failure 8 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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