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Summary Literature (0)
DOID:0070165 - spermatogenic failure 18

Disease Ontology Definition:A spermatogenic failure that is characterized by sperm flagellar morphological abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH1 gene on chromosome 3p21.

Synonyms: SPGF18

Xenbase Genes : dnah1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054615 - spermatogenic failure 18


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)