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Organizations

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This category in other languages:

Italian

Sites:

» American Society of Genetic Disorders Open in a new browser window - Informs health professionals, legislators, health policy makers, and the general public about all aspects of human genetics.
» Australian MPS & Related Diseases Society Open in a new browser window - Informs and support those affected, directly or indirectly by an mucopolysaccharide or related disease. Offers information regarding each disease, a discussion forum, a picture gallery and news of events.
» Dana's Angels Research Trust Open in a new browser window - Information from this charitable organization on Niemann-Pick Type C disease and how individuals can contribute funds for research for this fatal childhood disease.
» Genetic Interest Group Open in a new browser window - Information about this UK umbrella group of organizations working together to improve services for people with genetic disorders. A notice board, education, services and links are provided.
» Hereditary Disease Foundation Open in a new browser window - Information about this non profit organization, news, newsletters, recommended reading and contact details.
» Hereditary Hemorrhagic Telangiectasia Foundation International, Inc. Open in a new browser window - Provides patients, families, and doctors with educational information and fosters an exchange of information about the diagnosis and treatment of HHT between patients, physicians, researchers, genetic counselors, agencies, educators, and the general publi
» Lysosomal Diseases New Zealand Open in a new browser window - Information, support and advocacy for families affected by Lysosomal Storage Diseases, a group of rare genetic diseases.
» The Ryan Foundation Open in a new browser window - A non-profit, all-volunteer organization dedicated to supporting research for, and the families of, those suffering from Mucopolysaccharidosis, or MPS. Find disease info, articles and links.


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Last Updated: 2007-03-24 04:58:26


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