spermatogenic failure 17 Disease Ontology Browser

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spermatogenic failure 17 (DOID:0070174)
Alliance: disease page
Synonyms: Male infertility due to oocyte activation failure; SPGF17
Alt IDs: OMIM:617214
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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