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DO Term : spermatogenic failure 55 [DOID:0112337] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by male infertility due to asthenozoospermia, with severely reduced sperm motility that has_material_basis_in homozygous or compound heterozygous mutation in the SPAG17 gene on chromosome 1p12.
  • synonyms:
  • OMIM:619380,
  • 619380,
  • SPGF55
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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