malacards.org
malacards - human disease database
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Ranked 980st globally in Health Health Conditions and Concerns
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omim.org
online mendelian inheritance in man (omim) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. the full-text, referenced overviews in omim contain information on all known mendelian disorders and over 15,000 genes. omim focuses on the relationship between phenotype and genotype. it is updated daily, and the entries contain copious links to other genetics resources.
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rarediseases.org
nord, a 501(c)(3) organization, is the leading patient advocacy organization dedicated to improving the lives of individuals and families living with rare diseases.
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Ranked 13768st globally in Health Health Conditions and Concerns
orpha.net
the portal for rare diseases and orphan drugs
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earandsinusinstitute.com
marc dean, md is a board-certified otolaryngologist, practicing full time in private practice in fort worth, texas. call today to learn more!
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Ranked 502498st globally in Health Health Conditions and Concerns
globalgenes.org
global genes is committed to providing information, resources and connections to all communities affected by rare disease.
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abcd.care
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braintumourresearch.org
our vision is to find a cure for brain tumours. we are fundraising research at centres of excellence to help fight brain cancer.
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healthjade.net
lour goal is to provide you with scientifically proven healthy eating information and put them together for easy reading for you. happier and healthier!
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pancreasfoundation.org
npf patient registry learn more national pancreas foundation mission the national pancreas foundation provides hope for those suffering from pancreatitis and pancreatic cancer through funding cutting edge research, advocating for new and better therapies, and providing support and education for patients, caregivers, and health care professionals. donate today e-news sign-up stories patient/caregiver stories edmund’s story may 7, 2022/ my pancreatitis journey began in 2017;
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