Beckwith‑Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
Engelsk navn: Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
Engelske synonym: Mosaic paternal uniparental disomy of chromosome 11,UPD(11)pat
Definisjon
This disease is described under Beckwith-Wiedemann syndrome
Fra Orphanet
ORPHA: 96193
Klassifiseringsnivå: Subtype of disorder
ICD-10: Q87.3