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DO Term : X-linked spermatogenic failure 8 [DOID:0070599] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by sperm with head and midpiece defects, deformed and detached acrosomes, and markedly reduced progressive motility that has_material_basis_in hemizygous mutation in the CYLC1 gene on chromosome Xq21.1.
  • synonyms:
  • 301119,
  • OMIM:301119,
  • SPGFX8
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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