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Summary Literature (0)
DOID:0111922 - spermatogenic failure 31

Disease Ontology Definition:A male failure due to acephalic spermatozoa that is characterized by oligozoospermia with a high proportion of acephalic sperm that has_material_basis_in homozygous or compound heterozygous mutation in the PMFBP1 gene on chromosome 16q22.2.

Synonyms: SPGF31

Xenbase Genes : pmfbp1


MIM:
MIM:618112 - SPERMATOGENIC FAILURE 31; SPGF31

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)