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Prader-Willi Syndrome

Prevalence: 1/15000

neurological

Official·OMIM:176270 Official·ORPHA739

Neurodevelopmental disorder caused by loss of paternal allele at 15q11-q13.

Associated Genes

SNRPNSmall Nuclear Ribonucleoprotein Polypeptide N

Chromosome 15paternal_imprinting