Prader-Willisyndroom door paternale deletie van 15q11q13 type 1
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- Overerving
- Autosomal dominant
- Leeftijd van aanvang
- Antenatal, Neonatal
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1