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DOID:0112273 - spermatogenic failure 51
Disease Ontology Definition:A spermatogenic failure characterized by severe asthenoteratozoospermia with multiple morphologic abnormalities of the flagella resulting in reduced to absent motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP91 gene on chromosome 3q13.33.
Synonyms: SPGF51
Xenbase Genes

MIM:619177 - SPERMATOGENIC FAILURE 51; SPGF51 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee