Orphanet: Witteveen Kolk syndrome
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Witteveen-Kolk syndrome

Disease definition

A rare genetic neurodevelopmental syndrome characterized by mild intellectual disability, developmental delay, dysmorphic facial features, growth- and feeding problems, hypotonia, epilepsy, behavioral problems and a variety of congenital abnormalities.

ORPHA:500163

Classification level: Disorder
  • Synonym(s):
    • SIN3A-related intellectual disability syndrome
    • WITKOS
  • Prevalence: <1 / 1 000 000
  • Inheritance: -
  • Age of onset: Antenatal, Neonatal
  • ICD-10: -
  • OMIM: -
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -
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