U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Agammaglobulinemia 2, autosomal recessive

Agammaglobulinemia 2, autosomal recessive

Synonyms
AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT

Summary

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the IGLL1 gene. [from MONDO]

Available tests

19 tests are in the database for this condition.

Clinical tests (19 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: 14.1, AGM2, CD179b, IGL1, IGL5, IGLJ14.1, IGLL, IGO, IGVPB, VPREB2, IGLL1
    Summary: immunoglobulin lambda like polypeptide 1

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.