Search Ontology:
Human Disease
spermatogenic failure 7
- Term ID
- DOID:0070173
- Synonyms
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models