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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.
More at Wikipedia
Genomic imprinting
Angelman syndrome
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Epigenetics
ROHHAD
Medical conditions related to obesity
Genodermatoses
Syndromes
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