Search Ontology:
Human Disease

spermatogenic failure 59

Term ID
DOID:0112357
Synonyms
  • SPGF59
Definition
A spermatogenic failure that is characterized by male infertility due to nonobstructive azoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the TERB2 gene on chromosome 15q21.1. https://pubmed.ncbi.nlm.nih.gov/33211200/
References
Ontology
Human Disease   ( DOID:0112357 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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