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DO Term : spermatogenic failure 79 [DOID:0070578] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by an abnormal acrosome reaction and impaired membrane potential after capacitation that has_material_basis_in homozygous mutation in the KCNU1 gene on chromosome 8p11.23.
  • synonyms:
  • OMIM:620196,
  • SPGF79,
  • 620196
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Disease

Diseases --> Human genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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