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DO Term : agammaglobulinemia 4 [DOID:0060027] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An agammaglobulinemia that has_material_basis_in a mutation a homozygous mutation in the BLNK gene on chromosome 10q23.2.

synonyms:
OMIM:613502,
BLNK deficiency,
B-cell linker protein deficiency,
B cell linker protein deficiency,
613502

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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