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Rare disease
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Intellectual disability syndrome due to a DYRK1A point mutation
Intellectual disability syndrome due to a DYRK1A point mutation
ORPHA:
464311
· ICD-10
Q87.8
Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Infancy, Neonatal
ICD-10 Q87.8 →
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