Search Ontology:
Human Disease
spermatogenic failure 8
- Term ID
- DOID:0070169
- Synonyms
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- SPGF8
- Definition
- A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/20887963
- References
- Ontology
- Human Disease ( DOID:0070169 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models