Congenital anomaly of central nervous system
Congenital degeneration of nervous system
Pelizaeus-Merzbacher disease
X-linked recessive hereditary disease
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Pelizaeus-Merzbacher disease, connatal variant (disorder)
Pelizaeus-Merzbacher disease, connatal variant
Type II congenital Pelizaeus-Merzbacher disease
ziekte van Pelizaeus-Merzbacher type 2
PMD type 2
connatale vorm van Pelizaeus-Merzbacher-syndroom
Id59636002
StatusPrimitive
Associated morphologyMyelin sheath alteration
Finding siteMyelinated nerve fiber structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDystrophy
Finding siteWhite matter structure of brain and spinal cord
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetE75.2
RuleTRUE
AdviceALWAYS E75.2
CorrelationSNOMED CT source code to target map code correlation not specified