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DO Term : spermatogenic failure 44 [DOID:0112109] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by high prevalence of acephalic sperm and reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the CEP112 gene on chromosome 17q24.1.
  • synonyms:
  • 619044,
  • OMIM:619044,
  • SPGF44
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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