/agammaglobulinemia 5, autosomal dominant

agammaglobulinemia 5, autosomal dominant

Rare Disease

MONDO:0013290

Also Known As

LRRC8A autosomal agammaglobulinemiaagammaglobulinemia 5agammaglobulinemia 5, autosomal dominantautosomal agammaglobulinemia caused by mutation in LRRC8AAGM5agammaglobulinemia, autosomal dominant, due to Lrrc8A defect

Definition

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the LRRC8A gene.

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Associated Genes

LRRC8A ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:613506 ↗

GARD

GARD:15675 ↗

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