Search Ontology:
Human Disease

X-linked spermatogenic failure 5

Term ID
DOID:0070596
Synonyms
  • SPGFX5
Definition
A spermatogenic failure characterized by asthenoteratozoospermia with multiple morphologic abnormalities of the sperm flagella that has_material_basis_in hemizygous mutation in the SSX1 gene on chromosome Xp11.23. https://pubmed.ncbi.nlm.nih.gov/36796361/
References
Ontology
Human Disease   ( DOID:0070596 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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