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Summary Literature (0)
DOID:0070170 - spermatogenic failure 19

Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25.

Synonyms: SPGF19,

Xenbase Genes : cfap43

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054723 - spermatogenic failure 19


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), spermatogenic failure (is_a)