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DO Term : spermatogenic failure 36 [DOID:0111921] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by spermatozoa showing anomalies of the head, acrosome, and nucleus of the sperm resulting in reduced fertility that has_material_basis_in heterozygous mutation in the PPP2R3C gene on chromosome 14q13.2.
  • synonyms:
  • SPGF36,
  • OMIM:618420,
  • 618420
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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