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 null syndrome (disorder)
Pelizaeus-Merzbacher disease null syndrome
Null syndrome
PLP1 null syndrome
nulsyndroom bij ziekte van Pelizaeus-Merzbacher
PLP1-nulsyndroom
Id1003447007
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 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified