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DO Term : X-linked spermatogenic failure 3 [DOID:0112274] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by asthenoteratozoospermia with multiple morphologic abnormalities of the flagella that has_material_basis_in hemizygous mutation in the CFAP47 gene on chromosome Xp21.1.
  • synonyms:
  • 301059,
  • OMIM:301059,
  • SPGFX3
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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





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