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geïsoleerde hereditaire congenitale faciale paralyse (aandoening)
geïsoleerde hereditaire congenitale faciale paralyse
Isolated hereditary congenital facial paralysis
An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.
Id733091002
StatusPrimitive
Associated morphologyaplasia
Finding sitestructuur van nervus facialis
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
InterpretsMovement
referentieset met complexe 'mapping' naar ICD-10
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified