spermatogenic failure 13 Disease Ontology Browser

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Disease Ontology Browser

spermatogenic failure 13 (DOID:0070182)
Alliance: disease page
Synonyms: SPGF13
Alt IDs: OMIM:615841
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11.

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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