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Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency (disorder)
Combined immunodeficiency due to CARMIL2 deficiency
Combined immunodeficiency due to RLTPR deficiency
Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency
A rare immune dysregulation disease with immunodeficiency with characteristics of infantile or childhood onset of a variable phenotype including recurrent/persistent bacterial, fungal and viral infections with involvement of the skin, lower respiratory tract, gastrointestinal tract, eczema, allergies and inflammatory bowel disease. Epstein-Barr related smooth muscle neoplasms have also been reported. Immunophenotyping shows decreased Treg counts, as well as a deficient CD3/CD28 co-stimulation response in CD4+ and CD8+ T-cells.
gecombineerde immunodeficiëntie door CARMIL2-deficiëntie
gecombineerde immunodeficiëntie door deficiëntie van 'capping protein regulator and myosin 1 linker 2'
gecombineerde immuundeficiëntie door RLTPR-deficiëntie
Id1186712009
StatusPrimitive
Associated morphologyLymphoproliferative disorder
Pathological processDysregulated host response
ICD-10 complex map reference set
TargetD82.3
RuleTRUE
AdviceALWAYS D82.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified