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DO Term : spermatogenic failure 51 [DOID:0112273] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by severe asthenoteratozoospermia with multiple morphologic abnormalities of the flagella resulting in reduced to absent motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP91 gene on chromosome 3q13.33.
  • synonyms:
  • 619177,
  • OMIM:619177,
  • SPGF51
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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