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anhidrotische ectodermale dysplasie met immunodeficiƫntie door 'gain of function'-mutatie in 'inhibitor of nuclear factor kappa B kinase subunit beta' (aandoening)
anhidrotische ectodermale dysplasie met immunodeficiƫntie door 'gain of function'-mutatie in 'inhibitor of nuclear factor kappa B kinase subunit beta'
hyper-IgM-syndroom met hypohidrotische ectodermale dysplasie door GOF-mutatie in IKBKB
HED-ID door IKBKB-GOF-mutatie
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB gain of function mutation
Id1366698006
StatusPrimitive
Pathological processafwijkend immuunproces
Has interpretationafwijkend
Interpretszweten
Associated morphologydysplasie
Finding sitestructuur van ectoderm
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologymorfologische afwijking
Finding sitestructuur van haar
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to ICD-10 extended map
TargetQ82.4
RuleTRUE
AdviceALWAYS Q82.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified