| Term Name: | spermatogenic failure 48 |
|---|---|
| Synonyms: | SPGF48 |
| 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. |
| Ontology: | Human Disease [DOID:0112176] ( DOID:0112176 ) |