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Prader-Willi syndrome due to paternal 15q11q13 deletion
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ORPHA:98793
Classification level: Subtype of disorder
Prevalence: -
Inheritance: Autosomal dominant
Age of onset: Antenatal, Neonatal
Summary
This disease is described under Prader-Willi syndrome
Detailed information
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
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Research activities on this disease
- Research project(s) (58)
- Clinical trial(s) (9)
- Biobank(s) (15)
- Registry(ies) (33)
- Network of experts (5)
Newborn screening
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