Search Ontology:
Human Disease

spermatogenic failure 13

Term ID
DOID:0070182
Synonyms
  • SPGF13
Definition
A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11. https://www.ncbi.nlm.nih.gov/pubmed/24431330
References
Ontology
Human Disease   ( DOID:0070182 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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