Search Ontology:
Human Disease
spermatogenic failure 3
- Term ID
- DOID:0070168
- Synonyms
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- SPGF3
- Definition
- A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/23582645
- References
- Ontology
- Human Disease ( DOID:0070168 )
- is a type of
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