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syndroom van spinocerebellaire ataxie en dysmorfie (aandoening)
syndroom van spinocerebellaire ataxie en dysmorfie
Spinocerebellar ataxia dysmorphism syndrome
Syndrome that is marked by characteristic facies associated with dysarthria, delayed psychomotor development, ataxia, scoliosis and foot deformities. Three cases have been described and transmission appears to be autosomal recessive.
Id733033001
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van voet
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetG11.8
RuleTRUE
AdviceALWAYS G11.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified