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DO Term : X-linked spermatogenic failure 5 [DOID:0070596] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by asthenoteratozoospermia with multiple morphologic abnormalities of the sperm flagella that has_material_basis_in hemizygous mutation in the SSX1 gene on chromosome Xp11.23.
  • synonyms:
  • 301099,
  • OMIM:301099,
  • SPGFX5
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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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