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
This disease is described under Beckwith-Wiedemann syndrome
Informasjon
Frambu kompetansesenter for sjeldne diagnoser har kunnskap om diagnosen.
ORPHA: 96193
Klassifiseringsnivå: Subtype of disorderICD-10: Q87.3