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DOID:0070163 - spermatogenic failure 21
Disease Ontology Definition:A male infertility characterized by acephalic spermatozoa, reduced sperm number and impaired sperm motility that has_material_basis_in homozygous mutation in the BRDT gene on chromosome 1p22.
Synonyms:
Xenbase Genes : brdt
MONDO:0054725 - spermatogenic failure 21 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee