|OBO ID: DOID:0070163|
|Term Name:||spermatogenic failure 21||Search Ontology:|
|Definition:||A male infertility due to acephalic spermatozoa that is characterized by acephalic spermatozoa, reduced sperm number and impaired sperm motility that has_material_basis_in homozygous mutation in the BRDT gene on chromosome 1p22. https://www.ncbi.nlm.nih.gov/pubmed/28199965|
|Ontology:||Human Disease (DOID:0070163)|
|is a type of:||
OTHER spermatogenic failure 21 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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