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DO Term : agammaglobulinemia 8A [DOID:0081140] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13.

synonyms:
616941,
OMIM:616941

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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