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DO Term : spermatogenic failure 89 [DOID:0070588] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spermatogenic failure characterized by severely reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the AK9 gene on chromosome 6q21.

synonyms:
SPGF89,
620705,
OMIM:620705

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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