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Pediatric multiple sclerosis (disorder)
Pediatric multiple sclerosis
Pediatric multiple sclerosis (MS) is a rare multiple sclerosis variant characterized by the onset of multiple sclerosis (i.e. one or multiple episodes of clinical CNS symptoms consistent with acquired CNS demyelination, with radiologically proven dissemination of inflammatory lesions in space and time, following exclusion of other disorders) before the age of 18 years old. Pediatric MS patients present a predominantly relapsing-remitting course with first attack usually consisting of optic neuritis, transverse myelitis, acute disseminated encephalomyelitis and monofocal or polyfocal neurological deficits. A high burden of T2-hyperintense lesions on initial MRI, primarily of the supratentorial region and/or of the cervical spinal cord, has been reported.
Id1186728004
StatusPrimitive
Associated morphologyDemyelination
Finding siteStructure of central nervous system
OccurrenceChildhood
Pathological processAbnormal immune process
Associated morphologyInflammatory morphology
Finding siteStructure of central nervous system
OccurrenceChildhood
Pathological processAbnormal immune process
Clinical courseChronic
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetG35
TermMultipele sclerose
SNOMED CT to ICD-10 extended map
TargetG35
RuleTRUE
AdviceALWAYS G35 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified