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DO Term : spermatogenic failure 38 [DOID:0111919] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in infertility and asthenoteratozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC2 gene on chromosome 6q21.
  • synonyms:
  • OMIM:618433,
  • 618433,
  • SPGF38
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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