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Human Disease

spermatogenic failure 39

Term ID
DOID:0111926
Synonyms
  • SPGF39
Definition
A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3. https://pubmed.ncbi.nlm.nih.gov/31178125/
References
Ontology
Human Disease   ( DOID:0111926 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models