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Human Disease

spermatogenic failure 7

Term ID
DOID:0070173
Synonyms
  • SPGF7
Definition
A spermatogenic failure that is characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/19344877
References
Ontology
Human Disease   ( DOID:0070173 )
Relationships
is a type of
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Genes Involved
Zebrafish Models