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DO Term : spermatogenic failure 42 [DOID:0111923] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severly impaired sperm progressive motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC29 gene on chromosome 4q31.22.
  • synonyms:
  • 618745,
  • SPGF42,
  • OMIM:618745
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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