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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
Other Model Organisms: AGR, 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)