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Human Disease

spermatogenic failure 3

Term ID
DOID:0070168
Synonyms
  • SPGF3
Definition
A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/23582645
References
Ontology
Human Disease   ( DOID:0070168 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models