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Prader-Willi syndrome
Prader–Willi syndrome (; abbreviated PWS) is a rare genetic disorder in which seven genes (or some subset thereof) on chromosome 15 (q 11–13) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome.
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Genomic imprinting
Angelman syndrome
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Epigenetics
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Medical conditions related to obesity
Genodermatoses
Syndromes
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