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DO Term : spermatogenic failure 92 [DOID:0070591] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by asthenozoospermia that has_material_basis_in homozygous mutation in the LRRC23 gene on chromosome 12p13.31.
  • synonyms:
  • OMIM:620848,
  • SPGF92,
  • 620848
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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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