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DO Term : Y-linked spermatogenic failure 2 [DOID:0070187] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spermatogenic failure that is characterized by nonobstroctive azoospermia or oligozoospermia that has_material_basis_in interstitial deletions on the Yq11.221 chromosomal region.

synonyms:
SPGFY2,
nonobstructive Y-linked spermatogenic failure,
OMIM:415000,
415000,
MESH:C564030

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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