Search Ontology:
Human Disease

spermatogenic failure 12

Term ID
DOID:0070171
Synonyms
  • SPGF12
Definition
A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26. https://www.ncbi.nlm.nih.gov/pubmed/23315541
References
Ontology
Human Disease   ( DOID:0070171 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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