spermatogenic failure 38 Disease Ontology Browser

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spermatogenic failure 38 (DOID:0111919)
Alliance: disease page
Synonyms: SPGF38
Alt IDs: OMIM:618433
Definition: A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in infertility and asthenoteratozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC2 gene on chromosome 6q21.

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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