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DO Term : spermatogenic failure 35 [DOID:0111914] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 17q25.1.
  • synonyms:
  • SPGF35,
  • OMIM:618341,
  • 618341
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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