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Hermanski-Pudlak Syndrome
2 Diseases & Disorders / 2 Eye Diseases, Hereditary / 2 Albinism /  
2 Albinism, Oculocutaneous / Hermanski-Pudlak Syndrome
 
  MeSH description: Syndrome characterized by the triad of oculocutaneous albinism, platelet storage pool deficiency, and lysosomal accumulation of ceroid lipofuscin.
 
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