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DO Term : spermatogenic failure 82 [DOID:0070581] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella that has_material_basis_in homozygous mutation in the AKAP3 gene on chromosome 12p13.32.

synonyms:
620353,
SPGF82,
OMIM:620353

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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