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Summary Literature (0)
DOID:0070163 - spermatogenic failure 21

Disease Ontology Definition:A male infertility due to acephalic spermatozoa that is 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 Disease Ontology (on Monarch Initiative):
MONDO:0054725 - spermatogenic failure 21

MIM:
MIM:617644 - SPERMATOGENIC FAILURE 21; SPGF21

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), male infertility due to acephalic spermatozoa (is_a), spermatogenic failure (is_a)