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vatbaarheid voor infectie door deficiëntie van tyrosinekinase 2 (aandoening)
vatbaarheid voor infectie door deficiëntie van tyrosinekinase 2
autosomaal recessief hyperimmunoglobuline-E-syndroom door TYK2-deficiëntie
gevoeligheid voor infectie door TYK2-deficiëntie
Susceptibility to infection due to TYK2 deficiency
Autosomal recessive hyper-IgE (immunoglobulin E) syndrome due to TYK2 deficiency
Susceptibility to infection due to tyrosine kinase 2 deficiency
A rare primary immunodeficiency with characteristics of increased susceptibility to intracellular bacterial and viral infection, with or without increased serum immunoglobulin E. Clinical manifestations are highly variable, depending on the infection type and location, and can include recurrent otitis, sinusitis, pulmonary and cutaneous infections, meningitis and internal abscesses.
Id1197415001
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to Orphanet simple map331226
SNOMED CT to ICD-10 extended map
TargetD82.4
RuleTRUE
AdviceALWAYS D82.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified