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Persistent polyclonal B-cell lymphocytosis
1 OMIM reference -
1 associated gene
13 connected diseases
No signs/symptoms info
Disease Type of connection
Severe combined immunodeficiency due to CARD11 deficiency
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
MALT lymphoma
Autoimmune lymphoproliferative syndrome with recurrent infections
Autosomal dominant hypohidrotic ectodermal dysplasia
B-cell chronic lymphocytic leukemia
Cerebellar ataxia - hypogonadism
Mantle cell lymphoma
Multiple myeloma
Combined immunodeficiency due to ZAP70 deficiency
- Persistent polyclonal B-cell lymphocytosis with binucleated lymphocytes

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: no data available
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
CARD11 Q9BXL7607210
No signs/symptoms info available.