spermatogenic failure 22 Disease Ontology Browser

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Disease Ontology Browser

spermatogenic failure 22 (DOID:0070177)
Alliance: disease page
Synonyms: SPGF22
Alt IDs: OMIM:617706
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.

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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