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DO Term : spermatogenic failure 78 [DOID:0070577] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by sperm with abnormal acrosome structure due to a manchette assembly defect that has_material_basis_in homozygous mutation in the IQCN gene on chromosome 19p13.11.
  • synonyms:
  • OMIM:620170,
  • SPGF78,
  • 620170
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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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