OBO ID: DOID:0111926 |
Term Name: | spermatogenic failure 39 | Search Ontology: | |
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Synonyms: |
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Definition: | A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3. https://pubmed.ncbi.nlm.nih.gov/31178125/ | ||
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Ontology: | Human Disease ( DOID:0111926 ) |
OTHER spermatogenic failure 39 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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DNAH17 | Spermatogenic failure 39 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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