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Autosomal dominant spastic paraplegia type 79A (disorder)
Autosomal dominant spastic paraplegia type 79A
UCHL1-gene related autosomal dominant spastic paraplegia type 79
Autosomal dominant spastic paraplegia 79A with ataxia
SPG79A - spastic paraplegia type 79A
Id1375927000
StatusPrimitive
Clinical courseprogressief
Has interpretationafwezig
InterpretsMovement observable
SNOMED CT to ICD-10 extended map
TargetG11.4
RuleTRUE
AdviceALWAYS G11.4
CorrelationSNOMED CT source code to target map code correlation not specified