Category:Prader-Willi syndrome

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<nowiki>síndrome de Prader-Willi; پرادر ویلی سندرومو; Prader-Willi-Syndrom; Prader–Willi syndrome; نشانگان پرادرویلی; 普瑞德威利症候群; Prader-Willi syndrom; Prader Willi Sendromu; プラダー・ウィリー症候群; Prader-Willis syndrom; תסמונת פראדר וילי; 普瑞德威利症候群; प्रैड़र-विली सिंड्रोम; Prader–Willin oireyhtymä; Prader–Willi syndrome; Praderův-Williho syndrom; பிராடர் – வில்லி கூட்டறிகுறி; sindrome di Prader-Willi; syndrome de Prader-Willi; Prader Willi sindrom; 프래더-윌리 증후군; синдром Прадера-Віллі; sindromo de Prader-Willi; síndrome de Prader-Willi; síndrome de Prader Willi; Синдром на Прадер-Вили; Prader-Willi syndrom; Синдром Прадера — Вилли; Prader-Willijev sindrom; ପ୍ରେଡର-ଉଇଲି ସିଣ୍ଡ୍ରୋମ‎‎; Síndrome de Prader-Willi; Syndroom van Prader-Willi; กลุ่มอาการเพรเดอร์-วิลลี; Zespół Pradera-Williego; Prader-Willis syndrom; Prader-Villi sindromu; Прадер-Вилиев синдром; Hội chứng Prader–Willi; Պրադեր-Վիլի համախտանիշ; 普瑞德威利症候群; Prader–Willi syndrome; متلازمة برادر- فيلي; σύνδρομο Prader-Willi; Prader-Willijev sindrom; malattia genetica rara; maladie génétique rare; genetické onemocnění; zespół wad wrodzonych; הפרעה גנטית הגורמת לנזקים פיזיולוגיים; 遺傳性疾病; 遺傳性疾病; γενετική διαταραχή; Mutation des Chromosoms 15 mit körperlichen, stoffwechselbezogenen und kognitiven Symptomen; geneettinen oireyhtymä; 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; genetika malsano pri kromosomo 15; 遺傳性疾病; 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; Sindrome de Prader-Willi; zespół HHHO; Zespół Pradera-Williego-Labharta; Прадера-Віллі синдром; 小胖威利症; 小胖威利症; 小胖威利症; PWS; Prader-Williho syndrom; Prader Willi syndrome; Prader-Willi syndrome; PWS; Prader-Willi-sindromo; Σύνδρομο Πράντερ-Γουίλι; متلازمة برادر- ويلي</nowiki>
Prader-Willijev sindrom 
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
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Wikipodaci Q594013
GND: 4201277-6
LCCN: sh85106050
oznaka Nacionalne biblioteke Francuske: 12468434q
oznaka Parlamentarne biblioteke Japana: 01179976
BNCF pojmovnik: 67274
National Library of Israel J9U ID: 987007531653205171
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