Search Ontology:
Human Disease

spermatogenic failure 17

Term ID
DOID:0070174
Synonyms
  • Male infertility due to oocyte activation failure
  • SPGF17
Definition
A spermatogenic failure that is characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12. https://www.ncbi.nlm.nih.gov/pubmed/26721930
References
Ontology
Human Disease   ( DOID:0070174 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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