Agammaglobulinemia

finding

SNOMED 119249001CUI C0001768

Overview

Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.

Associated Conditions

Conditions associated with this symptom based on HPO disease-phenotype annotations.

X-linked agammaglobulinemia

Very frequent (80-99%)

Major histocompatibility complex class II deficiency

Deafness-dystonia syndrome

Occasional (5-29%)

Severe combined immunodeficiency with hypereosinophilia

Always present (100%)

Immunodeficiency, short limb dwarfism syndrome

Related Symptoms

Hypogammaglobulinemia Decreased alpha-globulin Alpha 1 globulin below reference range Decreased beta globulin Hypoglobulinaemia Hypoalphaglobulinaemia Cerebrospinal fluid globulin decreased Thyroxine binding globulin below reference range

Quick Facts

SNOMED CT: 119249001
UMLS CUI: C0001768
Fully Specified Name: Agammaglobulinemia (finding)
Associated Conditions: 5
Diagnostic Tests: 0

This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.