spermatogenic failure 23 Disease Ontology Browser

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Disease Ontology Browser

spermatogenic failure 23 (DOID:0070181)
Alliance: disease page
Synonyms: SPGF23
Alt IDs: OMIM:617707
Definition: A spermatogenic failure that is characterized by autosomal recessive inhertitance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23.

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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