Search Ontology:
Human Disease

spermatogenic failure 51

Term ID
DOID:0112273
Synonyms
  • SPGF51
Definition
A spermatogenic failure characterized by severe asthenoteratozoospermia with multiple morphologic abnormalities of the flagella resulting in reduced to absent motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP91 gene on chromosome 3q13.33. https://pubmed.ncbi.nlm.nih.gov/32161152/
References
Ontology
Human Disease   ( DOID:0112273 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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