|OBO ID: DOID:0111924|
|Term Name:||spermatogenic failure 26||Search Ontology:|
|Definition:||A spermatogenic failure due to acephalic spermatozoa that is characterized by acephalic spermatozoa due to breakage at the midpiece of the sperm that has_material_basis_in homozygous or compound heterozygous mutation in TSGA10 on chromosome 2q11.2. https://pubmed.ncbi.nlm.nih.gov/28905369/|
|Ontology:||Human Disease (DOID:0111924)|
|is a type of:||
OTHER spermatogenic failure 26 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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