Search Ontology:
Human Disease

spermatogenic failure 8

Term ID
DOID:0070169
Synonyms
  • 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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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