|OBO ID: DOID:0112176|
|Term Name:||spermatogenic failure 48||Search Ontology:|
|Definition:||A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1. (2)|
|Ontology:||Human Disease (DOID:0112176)|
|is a type of:||
OTHER spermatogenic failure 48 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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