Search Ontology:
Human Disease

X-linked spermatogenic failure 2

Term ID
DOID:0070185
Synonyms
  • SPGFX2
Definition
A spermatogenic failure that is characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13. https://www.ncbi.nlm.nih.gov/pubmed/25970010
References
Ontology
Human Disease   ( DOID:0070185 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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