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X-linked agammaglobulinemia

disorder
SNOMED 65880007CUI C0221026

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Clinical Trials

3
Total Trials
0
Recruiting
3
With Results

Recent Trials

A Study to Find Out How Safe and Effective Gammaplex® is in Young People With Primary Immunodeficiency

NCT01289847Phase 4Completed25 enrolled

Safety and Efficacy Study of Flebogamma 5% DIF IGIV in Pediatric Subjects

NCT00634569Phase 4Completed24 enrolled

Efficacy and Safety of Vivaglobin® in Previously Untreated Patients With Primary Immunodeficiency

NCT00520494Phase 4Completed18 enrolled
View all 3 trials on ClinicalTrials.gov

Signs & Symptoms

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

B cell lymphopenia
Always present (100%)HP:0010976
Complete or near-complete absence of specific antibody response to Haemophilus influenzae type b (Hib) vaccine
Always present (100%)HP:0410303
Constrictive bronchiolitis
Always present (100%)HP:0011946
Decreased circulating total IgM
Always present (100%)HP:0002850
IgE deficiency
Always present (100%)HP:0005479
Wheezing
Always present (100%)HP:0030828
Abnormality of the lymphatic system
Very frequent (80-99%)HP:0100763
Abnormality of the tonsils
Very frequent (80-99%)HP:0100765
Agammaglobulinaemia
Very frequent (80-99%)HP:0004432
Chronic diarrhoea
Very frequent (80-99%)HP:0002028
Chronic ear infection
Very frequent (80-99%)HP:0000389
Conjunctivitis
Very frequent (80-99%)HP:0000509
Decreased body height
Very frequent (80-99%)HP:0004322
Immune deficiency
Very frequent (80-99%)HP:0002721
Lower respiratory tract infections
Very frequent (80-99%)HP:0002783
Open skin sore
Very frequent (80-99%)HP:0200042
Pneumonia, recurrent
Very frequent (80-99%)HP:0006532
Poor weight gain
Very frequent (80-99%)HP:0001508
Posterior displacement of the tongue
Very frequent (80-99%)HP:0000162
Pyrexia
Very frequent (80-99%)HP:0001945
Recurrent cutaneous abscess formation
Very frequent (80-99%)HP:0100838
Sinus disease
Very frequent (80-99%)HP:0000246
Skin rash
Very frequent (80-99%)HP:0000988
Tiredness
Very frequent (80-99%)HP:0012378
Arthritis
Frequent (30-79%)HP:0001369
Bronchiectasis
Frequent (30-79%)HP:0002110
Decreased serum IgG
Frequent (30-79%)HP:0004315
Infection in blood stream
Frequent (30-79%)HP:0100806
Low blood calcium levels
Frequent (30-79%)HP:0002901
Low levels of immunoglobulin A
Frequent (30-79%)HP:0002720

Related Conditions

Hereditary disorder of immune system(parent)
X-linked hereditary disease(parent)
Isolated agammaglobulinaemia(parent)
Disorder of immune structure(parent)

Quick Facts

SNOMED CT
65880007
UMLS CUI
C0221026
Fully Specified Name
X-linked agammaglobulinemia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Clinical Trials
3
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.