Search Ontology:
Human Disease

spermatogenic failure 49

Term ID
DOID:0112271
Synonyms
  • SPGF98
Definition
A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella resulting in markedly reduced or no progressive motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP58 gene on chromosome 10q25.1. https://pubmed.ncbi.nlm.nih.gov/32791035/
References
Ontology
Human Disease   ( DOID:0112271 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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