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DO Term : spermatogenic failure 29 [DOID:0111930] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by nonobstructive azoospermia or oligozoospermia, immotile sperm, and sperm acrosome and head-neck junction abnormalities that has_material_basis_in homozygous or compound geterozygous mutation in the SPINK2 gene on chromosome 4q12.
  • synonyms:
  • SPGF29,
  • 618091,
  • OMIM:618091
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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