|  Help  |  About  |  Contact Us

DO Term : spermatogenic failure 12 [DOID:0070171] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • OMIM:615413,
  • 615413,
  • SPGF12
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents