Category:Prader-Willi syndrome

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síndrome de Prader-Willi (es); síndrome de Prader Willi (ca); Prader-Willi-Syndrom (de); Prader–Willi syndrome (en-gb); نشانگان پرادرویلی (fa); 普瑞德威利症候群 (zh); Prader Willi Sendromu (tr); プラダー・ウィリー症候群 (ja); Prader-Willis syndrom (sv); תסמונת פראדר וילי (he); 普瑞德威利症候群 (zh-hant); प्रैड़र-विली सिंड्रोम (hi); Prader–Willin oireyhtymä (fi); Prader–Willi syndrome (en-ca); Praderův-Williho syndrom (cs); பிராடர் – வில்லி கூட்டறிகுறி (ta); sindrome di Prader-Willi (it); syndrome de Prader-Willi (fr); Prader Willi sindrom (hr); 프래더-윌리 증후군 (ko); síndrome de Prader-Willi (pt); sindromo de Prader-Willi (eo); Պրադեր-Վիլի համախտանիշ (hy); 普瑞德威利症候群 (zh-tw); Синдром на Прадер-Вили (bg); Prader-Willijev sindrom (sl); Prader-Willi syndrom (nn); Síndrome de Prader-Willi (pt-br); Синдром Прадера — Вилли (ru); กลุ่มอาการเพรเดอร์-วิลลี (th); Zespół Pradera-Williego (pl); ପ୍ରେଡର-ଉଇଲି ସିଣ୍ଡ୍ରୋମ‎‎ (or); Prader-Villi sindromu (az); Syndroom van Prader-Willi (nl); синдром Прадера-Віллі (uk); Hội chứng Prader–Willi (vi); Прадер-Вили синдром (mk); Prader–Willi syndrome (en); متلازمة برادر- فيلي (ar); σύνδρομο Prader-Willi (el); Prader-Willijev sindrom (bs) malattia genetica rara (it); maladie génétique rare (fr); הפרעה גנטית הגורמת לנזקים פיזיולוגיים (he); 遺傳性疾病 (zh-tw); 遺傳性疾病 (zh-hant); 遺傳性疾病 (zh); Mutation des Chromosoms 15 mit körperlichen, stoffwechselbezogenen und kognitiven Symptomen (de); geneettinen oireyhtymä (fi); 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 (en); genetika malsano pri kromosomo 15 (eo); genetické onemocnění (cs); γενετική διαταραχή (el) Sindrome de Prader-Willi (es); zespół HHHO, Zespół Pradera-Williego-Labharta (pl); Прадера-Віллі синдром (uk); 小胖威利症 (zh-tw); 小胖威利症 (zh-hant); 小胖威利症 (zh); PWS, Prader-Williho syndrom (cs); Prader Willi syndrome, Prader-Willi syndrome, PWS (en); Prader-Willi-sindromo (eo); Σύνδρομο Πράντερ-Γουίλι (el); متلازمة برادر- ويلي (ar)
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
PWS8.png
Pws.jpg
Pws.svg
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Instance of
  • designated intractable/rare diseases
  • rare disease
  • class of disease
Subclass of
  • chromosomal disease
  • syndrome
  • syndromic obesity
  • disease (individual)
Named after
  • Andrea Prader
  • Heinrich Willi
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Subcategories

This category has the following 3 subcategories, out of 3 total.

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Media in category "Prader-Willi syndrome"

The following 14 files are in this category, out of 14 total.