autosomal agammaglobulinemia

MeSH: C538056ORPHA: 33110

Overview

group of hereditary diseases in humans

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with autosomal agammaglobulinemia, sourced from HPO and Orphanet clinical annotations.

High palateSinusitisEpicanthusHypertelorismChronic otitis mediaConjunctivitisSkin rashMeningitisArthritisFailure to thriveRecurrent skin infectionsDecreased total neutrophil countDehydrationFeverDiarrheaMalabsorptionBronchiectasisRecurrent respiratory infectionsRecurrent infectionsImmunodeficiencyOsteomyelitisAgammaglobulinemiaHepatitisFatigueCoughCellulitisSepsisVerrucaeAbnormal pinna morphology

Classification & Codes

MeSH Code

C538056

Orphanet Code

ORPHA:33110
autosomal agammaglobulinemia
MeSHC538056
OrphanetORPHA:33110
Treatments0 drug(s)
Symptoms on record29 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO