autosomaal dominante hereditaire aandoening
hereditaire ontwikkelingsstoornis
verbale ontwikkelingsdyspraxie
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Isolated childhood apraxia of speech (disorder)
Isolated childhood apraxia of speech
Speech-language disorder type 1
Isolated CAS (childhood apraxia of speech)
Speech and language disorder with orofacial dyspraxia
Isolated developmental verbal dyspraxia
Pure CAS (childhood apraxia of speech)
Pure childhood apraxia of speech
A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
Id1365977003
StatusPrimitive
InterpretsMotor function
Pathological processproces van pathologische ontwikkeling
Has interpretationafwijkend
Interpretsvermogen tot uitvoeren van functies gerelateerd aan communicatie
SNOMED CT to ICD-10 extended map
TargetF80.0
RuleTRUE
AdviceALWAYS F80.0
CorrelationSNOMED CT source code to target map code correlation not specified