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DO Term : spermatogenic failure 41 [DOID:0111912] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2.
  • synonyms:
  • SPGF41,
  • OMIM:618670,
  • 618670
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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