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Hyperimmunoglobulin M syndrome type 3

disorder
SNOMED 1362020006CUI C1720957

Overview

Hyperimmunoglobulin M syndrome type 3 is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Decreased serum IgG
HP:0004315
IgE deficiency
HP:0005479
Immune deficiency
HP:0002721
Impaired Ig class switch recombination
HP:0002959
Impaired memory B cell generation
HP:0002847
Increased IgM levels
HP:0003496
Low levels of immunoglobulin A
HP:0002720
Lymph nodes lack germinal center
HP:0002849
Neutropoenia
HP:0001875
Susceptibility to pyogenic infection
HP:0002718

Quick Facts

SNOMED CT
1362020006
UMLS CUI
C1720957
Fully Specified Name
Hyperimmunoglobulin M syndrome type 3 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
10
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.