Search Ontology:
Human Disease
spermatogenic failure 11
- Term ID
- DOID:0070180
- Synonyms
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- SPGF11
- Definition
- A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/17047026
- References
- Ontology
- Human Disease ( DOID:0070180 )
- is a type of
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Genes Involved
Zebrafish Models