Search Ontology:
Human Disease

X-linked spermatogenic failure 3

Term ID
DOID:0112274
Synonyms
  • SPGFX3
Definition
A spermatogenic failure characterized by asthenoteratozoospermia with multiple morphologic abnormalities of the flagella that has_material_basis_in hemizygous mutation in the CFAP47 gene on chromosome Xp21.1. https://pubmed.ncbi.nlm.nih.gov/33472045/
References
Ontology
Human Disease   ( DOID:0112274 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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