|OBO ID: DOID:0070182|
|Term Name:||spermatogenic failure 13||Search Ontology:|
|Definition:||A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11. https://www.ncbi.nlm.nih.gov/pubmed/24431330|
|Ontology:||Human Disease (DOID:0070182)|
|is a type of:||
OTHER spermatogenic failure 13 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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