spermatogenic failure 32 Disease Ontology Browser

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spermatogenic failure 32 (DOID:0111925)
Alliance: disease page
Synonyms: SPGF32
Alt IDs: OMIM:618115
Definition: A spermatogenic failure characterized by nonobstructive azoospermia, absence of spermatogenic cells and a Sertoli cell-only phenotype in testes that has_material_basis_in heterozygous mutation in the SOHLH1 gene on chromosome 9q34.3.

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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