Search Ontology:
Human Disease

spermatogenic failure 41

Term ID
DOID:0111912
Synonyms
  • SPGF41
Definition
A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2. https://pubmed.ncbi.nlm.nih.gov/31621862/
References
Ontology
Human Disease   ( DOID:0111912 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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