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DO Term : common variable immunodeficiency 14 [DOID:0081156] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the IRF2BP2 gene on chromosome 1q42.

synonyms:
OMIM:617765,
617765

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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