Prader–Willi syndrome (Q594013)

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genetic disorder on chromosome 15, causing weak muscles, slow development, obesity, intellectual impairment, narrow forehead, small hands/feet, short height, light skin/hair, and infertility
  • Prader Willi syndrome
  • Prader-Willi syndrome
  • PWS
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Language Label Description Also known as
English
Prader–Willi syndrome
genetic disorder on chromosome 15, causing weak muscles, slow development, obesity, intellectual impairment, narrow forehead, small hands/feet, short height, light skin/hair, and infertility
  • Prader Willi syndrome
  • Prader-Willi syndrome
  • PWS

Statements

PWS8.png
572 × 903; 420 KB
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Mardin P1050311 20080426123001.JPG
2,304 × 3,072; 2.86 MB
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Prader-WilliBMC.png
587 × 809; 610 KB
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Prader willi syndrome.webm
7 min 52 s, 1,920 × 1,080; 39.69 MB
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Pws.jpg
720 × 540; 72 KB
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Pws.svg
309 × 584; 414 KB
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Identifiers

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Sindrome di Prader-Willi
Sindrome di Prader Willi
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LD90.3
Prader-Willi syndrome
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Prader-Willin oireyhtymä
Prader-Willis syndrom
Prader-Willi syndrome
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