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Human Disease

spermatogenic failure 32

Term ID
DOID:0111925
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models