OBO ID: DOID:0111916 |
Term Name: | spermatogenic failure 28 | Search Ontology: | |
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Definition: | A spermatogenic failure characterized by nonobstructive azoospermia and a Sertoli cell-only phenotype in testes that has_material_basis_in homozygous or compound heterozygous mutation in the FANCM gene on chromosome 14q21.2. https://pubmed.ncbi.nlm.nih.gov/30075111/ | ||
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Ontology: | Human Disease ( DOID:0111916 ) |
OTHER spermatogenic failure 28 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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