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DO Term : spermatogenic failure 90 [DOID:0070589] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spermatogenic failure characterized by asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC12 gene on chromosome 6p21.31.

synonyms:
SPGF90,
620744,
OMIM:620744

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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