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DO Term : spermatogenic failure 52 [DOID:0112270] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure that is characterized by non-obstructive azoospermia resulting from meiotic arrest at the spermatocyte stage that has_material_basis_in homozygous or compound heterozygous mutation in C14orf39 on chromosome 14q23.1.
  • synonyms:
  • OMIM:619202,
  • 619202,
  • SPGF52
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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