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ontwikkelingsachterstand met autismespectrumstoornis en onvastheid bij lopen (aandoening)
ontwikkelingsachterstand met autismespectrumstoornis en onvastheid bij lopen
Developmental delay with autism spectrum disorder and gait instability
A rare genetic neurological disorder characterized by infant hypotonia and feeding difficulties, global development delay, mild to moderate intellectual disability, delayed independent ambulation, broad-based gait with arms upheld and flexed at the elbow with brisk walking or running, and limited language skills. Behavior patterns are highly variable and range from sociable and affectionate to autistic behavior. Caused by homozygous mutation in the HERC2 gene on chromosome 15q13.
Id770790004
StatusPrimitive
referentieset met complexe 'mapping' naar ICD-10
TargetF84.0
RuleTRUE
AdviceALWAYS F84.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetF89
RuleTRUE
AdviceALWAYS F89
CorrelationSNOMED CT source code to target map code correlation not specified
TargetR26.8
RuleTRUE
AdviceALWAYS R26.8
CorrelationSNOMED CT source code to target map code correlation not specified