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Prader-Willi Syndrome
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
SNRPN
Small Nuclear Ribonucleoprotein Polypeptide N
Chromosome 15
paternal_imprinting