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DO Term : spermatogenic failure 39 [DOID:0111926] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3.
  • synonyms:
  • SPGF39,
  • 618643,
  • OMIM:618643
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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