Syndroom van Beckwith-Wiedemann door CDKN1C-mutatie
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Overerving
- Autosomal dominant
- Leeftijd van aanvang
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation