Search Ontology:
Human Disease

spermatogenic failure 22

Term ID
DOID:0070177
Synonyms
  • SPGF22
Definition
A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/28206990
References
Ontology
Human Disease   ( DOID:0070177 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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