CentoMD\u00ae<\/a> Cuenta con datos de m\u00e1s de cinco millones de alelos in\u00e9ditos. Para cada individuo, proporciona informaci\u00f3n sobre la correlaci\u00f3n genotipo-fenotipo basada en casos cl\u00ednicos analizados.<\/p>\n\u201cSi bien cualquier enfermedad rara afecta solo a un peque\u00f1o porcentaje de personas, m\u00e1s de 350 millones de personas en todo el mundo las padecen. Diagnosticar a un paciente con una enfermedad rara puede ser extremadamente complejo y desafiante, ya que nuestra capacidad para descubrir una variaci\u00f3n gen\u00e9tica en el genoma de un paciente es superior a nuestra capacidad para interpretar dicha variaci\u00f3n. Alcanzar m\u00e1s de mil millones de alelos en nuestra base de datos CentoMD\u00ae es un hito enorme y mejorar\u00e1 significativamente la calidad de cualquier conjunto de datos gen\u00e9ticos, siendo la base para la atenci\u00f3n m\u00e9dica futura, afirm\u00f3 el profesor. Arndt Rolfs, director ejecutivo de CENTOGENE<\/strong>. Con esta informaci\u00f3n, los profesionales sanitarios y las empresas farmac\u00e9uticas asociadas podr\u00e1n determinar el diagn\u00f3stico m\u00e1s preciso y, en \u00faltima instancia, contribuir a acortar la distancia entre el diagn\u00f3stico y el tratamiento.\u201c<\/p>","protected":false},"excerpt":{"rendered":"CentoMD\u00ae es la base de datos global de mutaciones m\u00e1s grande del mundo para trastornos gen\u00e9ticos raros, que abarca m\u00e1s de 3300 fenotipos asociados de pacientes en 115 pa\u00edses. Descubra c\u00f3mo proporciona informaci\u00f3n sobre la correlaci\u00f3n genotipo-fenotipo basada en casos cl\u00ednicos comprobados.<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-2424","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"acf":[],"yoast_head":"\n
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