OBO ID: DOID:0112271 |
Term Name: | spermatogenic failure 49 | Search Ontology: | |
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Definition: | A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella resulting in markedly reduced or no progressive motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP58 gene on chromosome 10q25.1. https://pubmed.ncbi.nlm.nih.gov/32791035/ | ||
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Ontology: | Human Disease ( DOID:0112271 ) |
OTHER spermatogenic failure 49 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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