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DO Term : spermatogenic failure 86 [DOID:0070585] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by acrosomal defects of the spermatozoa, resulting in oocyte activation deficiency and fertilization failure, that has_material_basis_in homozygous or compound heterozygous mutation in the ACTL7A gene on chromosome 9q31.3.
  • synonyms:
  • 620499,
  • SPGF86,
  • OMIM:620499
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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