Search Ontology:
Human Disease
spermatogenic failure 32
- Term ID
- DOID:0111925
- Synonyms
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- SPGF32
- Definition
- A spermatogenic failure characterized by nonobstructive azoospermia, absence of spermatogenic cells and a Sertoli cell-only phenotype in testes that has_material_basis_in heterozygous mutation in the SOHLH1 gene on chromosome 9q34.3. https://pubmed.ncbi.nlm.nih.gov/20506135/
- References
- Ontology
- Human Disease ( DOID:0111925 )
- is a type of
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Genes Involved
Zebrafish Models