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DO Term : spermatogenic failure 59 [DOID:0112357] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spermatogenic failure that is characterized by male infertility due to nonobstructive azoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the TERB2 gene on chromosome 15q21.1.

synonyms:
SPGF59,
619645,
OMIM:619645

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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