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英文字典中文字典相关资料:


  • Genetic and Rare Diseases Information Center | GARD
    GARD provides access to information and resources that are current, reliable, and clear Using the support GARD offers can help ensure you are getting the best possible care for your rare disease
  • Diseases | GARD
    Browse by Disease Explore GARD's list of rare diseases Filter by category or search by disease name, acronym, or synonym Rare diseases found on GARD should not be used as policy statements of NCATS or the NIH
  • About | GARD - Genetic and Rare Diseases Information Center
    Learn about the Genetic and Rare Diseases Information Center, the GARD website and its policies, and how to access data used on the GARD website
  • Contact Us | GARD - Genetic and Rare Diseases Information Center
    We invite patients, family members, caregivers, and others seeking information about rare diseases to contact GARD by phone or through our contact form Our Information Specialists provide personalized responses that are easy to understand, free of charge, and confidential
  • Resources | GARD - Genetic and Rare Diseases Information Center
    Whether you're a patient or caregiver, GARD can help connect you with the resources and support you need to navigate life with a rare disease Please note that GARD provides organizations and resources for informational purposes only
  • Myofibrillar myopathy | About the Disease | GARD
    Symptoms: May start to appear as an Adult Cause: This disease is caused by a change in the genetic material (DNA) Organizations: Patient organizations dedicated to this rare disease are available on GARD, or you may contact a GARD Information Specialist for additional information Categories: Genetic diseases Neurological diseases
  • Centro de Información sobre Enfermedades Raras y Genéticas | GARD
    GARD brinda acceso a información y recursos actuales, confiables y claros Utilizar el respaldo que GARD ofrece puede contribuir a asegurar que reciba la mejor atención posible para su enfermedad rara
  • Campomelic dysplasia | About the Disease | GARD
    GARD uses data collected from Orphanet, Online Mendelian Inheritance in Man (OMIM) , and Mondo Disease Ontology to interpret and provide information on rare diseases
  • Peters anomaly | About the Disease | GARD
    Symptoms: May start to appear as a Newborn and as an Infant Cause: This disease is caused by a change in the genetic material (DNA) Organizations: Contact GARD Information Specialist to help search for patient organizations dedicated to this rare disease Categories: Genetic diseases Birth defects
  • Cloves syndrome | About the Disease | GARD
    Contact a GARD Information Specialist for help finding an expert You can ask your care providers for help finding an expert or use directory tools to search for experts near you The following organization (s) may maintain a list of experts or expert centers for people living with Cloves syndrome:





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