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DO Term : spermatogenic failure 2 [DOID:0070164] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spermatogenic failure that is characterized by azoospermia or severe oligozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the MSH4 gene on chromosome 1p31.

synonyms:
SPGF2,
OMIM:108420,
108420

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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