OBO ID: DOID:0111925
Term Name: spermatogenic failure 32 Search Ontology:
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:
OTHER spermatogenic failure 32 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SOHLH1 Spermatogenic failure 32
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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