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DO Term : X-linked spermatogenic failure 2 [DOID:0070185] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure that is characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13.
  • synonyms:
  • OMIM:309120,
  • 309120,
  • SPGFX2
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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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