Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Autoimmunity
Very frequent (80-99%)HP:0002960
Chronic noninfectious lymphadenopathy
Very frequent (80-99%)HP:0002730
Large spleen
Very frequent (80-99%)HP:0001744
Lymph node hyperplasia
Very frequent (80-99%)HP:0002716
Abnormal T cell apoptosis
Frequent (30-79%)HP:0030886
Abnormality of interleukin secretion
Frequent (30-79%)HP:0011117
Autoimmune haemolytic anemia
Frequent (30-79%)HP:0001890
Bleeding tendency
Frequent (30-79%)HP:0001892
Bruising susceptibility
Frequent (30-79%)HP:0000978
Enlarged liver
Frequent (30-79%)HP:0002240
Hyperglobulinemia
Frequent (30-79%)HP:0010702
Hypersplenism
Frequent (30-79%)HP:0001971
Immune thrombocytopenia
Frequent (30-79%)HP:0001973
Increased circulating interleukin 10 concentration
Frequent (30-79%)HP:0033199
Increased number of B cells
Frequent (30-79%)HP:0005404
Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors
Frequent (30-79%)HP:0002851
Increased total IgG in blood
Frequent (30-79%)HP:0003237
Neutropenia in presence of anti-neutropil antibodies
Frequent (30-79%)HP:0001904
Abnormal CD4+ T cell subset proportion
Occasional (5-29%)HP:0031392
Abnormal CD8+ T cell proportion
Occasional (5-29%)HP:0031393
Abnormal vitamin B12 level
Occasional (5-29%)HP:0040126
Absolute lymphocyte count decrease
Occasional (5-29%)HP:0001888
Antineutrophil antibody positivity
Occasional (5-29%)HP:0003453
Antinuclear antibodies
Occasional (5-29%)HP:0003493
Antiphospholipid antibodies
Occasional (5-29%)HP:0003613
B-cell lymphoma
Occasional (5-29%)HP:0012191
Burkitt lymphoma
Occasional (5-29%)HP:0030080
Decreased circulating total IgM
Occasional (5-29%)HP:0002850
Decreased proportion of CD4-positive T cells
Occasional (5-29%)HP:0032218
Decreased serum IgG
Occasional (5-29%)HP:0004315
Related Conditions
CTLA-4 haploinsufficiency with autoimmune infiltration disease(child)
STAT3-related early-onset multisystem autoimmune disease(child)
Hereditary disorder of immune system(parent)
Disorder of immune structure(parent)
Primary immune deficiency disorder(parent)
Autosomal hereditary disorder(parent)
Hereditary neoplastic syndrome(parent)
Lymphoproliferative disorder(parent)
Disorder of hematopoietic structure(parent)
Quick Facts
- SNOMED CT
- 702444009
- UMLS CUI
- C1328840
- Fully Specified Name
- Autoimmune lymphoproliferative syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.