spermatogenic failure 3 Disease Ontology Browser

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Disease Ontology Browser

spermatogenic failure 3 (DOID:0070168)
Alliance: disease page
Synonyms: SPGF3
Alt IDs: OMIM:606766
Definition: A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21.

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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