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Isolated hereditary congenital facial paralysis (disorder)
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.
geïsoleerde hereditaire congenitale faciale paralyse
Id733091002
StatusPrimitive
Has interpretationAbsent
InterpretsGross movement of body and limbs
Associated morphologyAplasia
Finding siteFacial nerve structure
OccurrenceCongenital
Pathological processPathological developmental process
InterpretsMovement
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
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