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You are here: Home : Diseases and Conditions : Genetic Disorders
Genetic Disorders
Select a Genetic Disorders Subcategories
Alpha-1 Antitrypsin Deficiency Organizations
Batten Personal Pages
Cystic Fibrosis Prader-Willi Syndrome
Down Syndrome Sanfilippo Syndrome
Ectodermal Dysplasia Shwachman Syndrome
Fragile X Syndrome Turner Syndrome
Hemochromatosis Urea Cycle
Hereditary Spastic Paraplegia Williams Syndrome
Klinefelter Syndrome Xeroderma Pigmentosum
Opitz Syndrome
Genetic Disorders Listings :
International Joseph Disease Foundation
Offers education, medical referrals, up-dates, and support to all individuals interested in Machado-Joseph Disease.
Nail Patella Syndrome Worldwide
The home page of Nail-Patella Syndrome Worldwide, the only non-profit serving the needs of people with Nail-Patella Syndrome. Includes information on the syndrome and the work of the organization.
Proteus Syndrome Foundation
Support and education for families and professionals. Includes abstracts, brochures, glossary, links and newsletters.
Rett Syndrome Association (UK)
The Rett Syndrome Association UK, a registered charity, is dedicated to the support of girls and women, together with their families and carers, suffering from this complex neurological disorder, which affects them throughout their lives. Sufferers are profoundly and multiply disabled.
Fatty Oxidation Disorders
Informational site provides details on newborn screening, on numerous diseases, medical information and support resources such as a newsletter and email List.
The Noonan Syndrome Support Group
Information about this organization as well the disease itself. Offers news, events, a survey, a newsletter and further resources.
Robinow Syndrome Foundation
Details about the organization as well as the disease. Includes general information, a survey, newsletter and photos.
PXE International
The comprehensive source for pseudoxanthoma elasticum research and world wide activities.
Hereditary Angioedema Support Group
A non profit Organization dedicated to those families that are touched by a rare blood disease known as Hereditary Angioedema
Laurence Moon Bardet Biedl Society
Fully accessible site for people with LMBB, their families, friends, carers and interested professionals. Opinions, news, views, research, updates, and contact details.

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