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syndroom van atopie geassocieerd met 'caspase recruitment domain family member 11' met dominante interferentie van nucleaire factor kappa-B-signalering (aandoening)
CADINS-ziekte
syndroom van atopie geassocieerd met 'caspase recruitment domain family member 11' met dominante interferentie van nucleaire factor kappa-B-signalering
syndroom van CARD11-geassocieerde atopie met dominante interferentie van nucleaire factor kappa-B-signalering
CADINS disease
CARD11-associated atopy with dominant interference of NF-kB signaling syndrome
Caspase recruitment domain family member 11-associated atopy with dominant interference of nuclear factor kappa-B signaling syndrome
A rare hyper-IgE syndrome characterized by early-onset moderate to severe atopic dermatitis and recurrent infections of variable severity including molluscum contagiosum, pneumonia, abscesses, bacteremia, or eczema herpeticum, among others. Other reported manifestations include asthma, food allergies, colitis, chronic diarrhea, lymphoma, and seizures, as well as dysmorphic facial features, such as prominent forehead, broad nose, and poor dentition.
Id1336113009
StatusPrimitive
Associated withatopie
Pathological processafwijkend immuunproces
Associated morphologyinflammatoire morfologie
Finding sitestructuur van huid
SNOMED CT to ICD-10 extended map
TargetD81.8
RuleTRUE
AdviceALWAYS D81.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified