Search Ontology:
Human Disease
spermatogenic failure 23
- Term ID
- DOID:0070181
- Synonyms
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- SPGF23
- Definition
- A spermatogenic failure that is characterized by autosomal recessive inhertitance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23. https://www.ncbi.nlm.nih.gov/pubmed/28206990
- References
- Ontology
- Human Disease ( DOID:0070181 )
- is a type of
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Genes Involved
Zebrafish Models