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DO Term : spermatogenic failure 22 [DOID:0070177] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.
  • synonyms:
  • OMIM:617706,
  • 617706,
  • SPGF22
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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