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Up to: Syndromic disease · Hereditary neurological disease

Angelman syndrome

A neurogenetic disorder characterized by severe intellectual deficit and distinct facial dysmorphic features.

19 trials tagged with this condition →

  • Angelman syndrome due to a point mutation 0 trials
  • Angelman syndrome due to imprinting defect in 15q11-q13 0 trials
  • Angelman syndrome due to maternal 15q11q13 deletion 0 trials
  • Angelman syndrome due to paternal uniparental disomy of chromosome 15 0 trials

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