autosomaal dominante hereditaire aandoening
hereditaire aandoening van immuunsysteem
hereditaire aandoening van zenuwstelsel
meningitis door herpes-simplexvirus type 2
primaire immunodeficiëntie
recidiverende herpes simplex
Recurrent meningitis
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Recurrent herpes simplex virus 2 meningitis due to autosomal dominant autophagy related 4A cysteine peptidase deficiency (disorder)
Recurrent HSV-2 (herpes simplex virus 2) meningitis due to autosomal dominant ATG4A deficiency
Recurrent herpes simplex virus 2 meningitis due to autosomal dominant autophagy related 4A cysteine peptidase deficiency
Recurrent herpes simplex virus 2 meningitis due to autosomal dominant ATG4A deficiency
Id1371052007
StatusPrimitive
Clinical courserecidiverend
Pathological processafwijkend immuunproces
Associated morphologyinflammatoire morfologie
Causative agentherpes-simplexvirus type 2
Finding sitestructuur van meningen
Pathological processinfectieus proces
SNOMED CT to ICD-10 extended map
TargetB00.3
RuleTRUE
AdviceALWAYS B00.3
CorrelationSNOMED CT source code to target map code correlation not specified
TargetG02.0
RuleTRUE
AdviceALWAYS G02.0 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified
TargetD84.8
RuleTRUE
AdviceALWAYS D84.8
CorrelationSNOMED CT source code to target map code correlation not specified