spermatogenic failure 11 Disease Ontology Browser

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Disease Ontology Browser

spermatogenic failure 11 (DOID:0070180)
Alliance: disease page
Synonyms: SPGF11
Alt IDs: OMIM:615081
Definition: A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21.

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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