Clinical Trials
3
Total Trials
1
Recruiting
2
With Results
Recent Trials
Immune Disorder HSCT Protocol
NCT01821781Phase 2Active Not Recruiting20 enrolled
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
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased mean platelet volume
Always present (100%)HP:0005537
Reduced natural killer cell activity
Always present (100%)HP:0012177
Abnormal shape of platelets
Very frequent (80-99%)HP:0011875
Absolute lymphocyte count decrease
Very frequent (80-99%)HP:0001888
Bruising susceptibility
Very frequent (80-99%)HP:0000978
Chronic diarrhoea
Very frequent (80-99%)HP:0002028
Chronic ear infection
Very frequent (80-99%)HP:0000389
COPD
Very frequent (80-99%)HP:0006510
High immunoglobulin E
Very frequent (80-99%)HP:0003212
Immune deficiency
Very frequent (80-99%)HP:0002721
Increased bleeding time
Very frequent (80-99%)HP:0003010
Internal bleeding
Very frequent (80-99%)HP:0011029
Otitis media
Very frequent (80-99%)HP:0000388
Pyrexia
Very frequent (80-99%)HP:0001945
respiratory infections, recurrent
Very frequent (80-99%)HP:0002205
Sinusitis
Very frequent (80-99%)HP:0000246
Spontaneous hematomas
Very frequent (80-99%)HP:0007420
Thrombocytopenia
Very frequent (80-99%)HP:0001873
Abnormal heart rate
Frequent (30-79%)HP:0011675
Abnormality of eosinophils
Frequent (30-79%)HP:0001879
Autoimmune disorder
Frequent (30-79%)HP:0002960
Blood spots
Frequent (30-79%)HP:0000979
Decreased circulating total IgM
Frequent (30-79%)HP:0002850
Decreased proportion of CD8-positive T cells
Frequent (30-79%)HP:0005415
Difficulty breathing
Frequent (30-79%)HP:0002094
Eosinophilia
Frequent (30-79%)HP:0001880
Hematemesis
Frequent (30-79%)HP:0002248
Hematochezia
Frequent (30-79%)HP:0002573
Hemolytic anaemia
Frequent (30-79%)HP:0001878
Impaired lymphocyte transformation with phytohemagglutinin
Frequent (30-79%)HP:0003347
Related Conditions
Wiskott-Aldrich autosomal dominant variant syndrome(child)
Dense body defect(parent)
Immunodeficiency associated with multiple organ system abnormalities(parent)
Hereditary disorder of immune system(parent)
Congenital immunodeficiency disease(parent)
Hereditary thrombocytopenic disorder(parent)
Hereditary neoplastic syndrome(parent)
Congenital thrombocytopenia(parent)
Thrombocytopenia due to immune destruction(parent)
Quick Facts
- SNOMED CT
- 36070007
- UMLS CUI
- C0043194
- Fully Specified Name
- Wiskott-Aldrich syndrome (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.