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DO Term : spermatogenic failure 5 [DOID:0070183] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure that is characterized by autosomal recessive inheritance of large-headed, multiflagellar, polyploid spermatozoa that has_material_basis_in mutation in the AURKC gene on chromosome 19q13.
  • synonyms:
  • SNOMEDCT_US_2021_09_01:236806004,
  • male infertility due to macrozoospermia,
  • ORDO:137893,
  • infertility associated with multitailed spermatozoa and excessive DNA,
  • male infertility with large-headed, multiflagellar, polyploid spermatozoa,
  • GARD:12385,
  • MESH:C562903,
  • SPGF5,
  • 243060,
  • OMIM:243060,
  • Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid,
  • macrocephalic sperm head syndrome
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Disease

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Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents