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Category List - Main » Health » Conditions and Diseases » Genetic Disorders

Aarskog Syndrome	Aase Syndrome
Ablepharon-Macrostomia Syndrome	Alagille Syndrome
Alkaptonuria	Alpha-1 Antitrypsin Deficiency
Batten	Beckwith-Wiedemann Syndrome
Coffin Lowry Syndrome	Costello Syndrome
Cowden Syndrome	Craniofrontonasal Dysplasia
Crigler-Najjar Syndrome	Cystic Fibrosis
DiGeorge Syndrome	Down Syndrome
Dubowitz Syndrome	Ectodermal Dysplasia
Familial Hypercholesterolemia	Fatty Oxidation
Floating-Harbor Syndrome	Fragile X Syndrome
Glutaricaciduria	Hailey-Hailey Disease
Hemihypertrophy	Hemochromatosis
Hereditary Angioedema	Hereditary Spastic Paraplegia
Incontinentia Pigmenti	Joubert Syndrome
Klinefelter Syndrome	Laurence-Moon Syndrome
Lesch-Nyhan Syndrome	Lowe Syndrome
Machado-Joseph	Mannosidosis
McArdle's	Meckel-Gruber Syndrome
Mobius Syndrome	Nail Patella Syndrome
Noonan Syndrome	Opitz Syndrome
Organizations	Pallister Killian Mosaic Syndrome
Pallister-Hall Syndrome	Personal Pages
Popliteal Pterygium Syndrome	Prader-Willi Syndrome
Propionic Acidemia	Proteus Syndrome
Prune Belly Syndrome	Pseudoxanthoma Elasticum
Robinow Syndrome	Russell Silver Syndrome
Sanfilippo Syndrome	Schizencephaly
Shwachman Syndrome	Smith Lemli Opitz Syndrome
Smith-Magenis Syndrome	Soto's Syndrome
Sturge-Weber Syndrome	Thrombocytopenia Absent Radius Syndrome
Turner Syndrome	Urea Cycle
Usher Syndrome	Velo-Cardio-Facial Syndrome
Von Hippel-Lindau	Waardenburg Syndrome
Weaver Syndrome	Williams Syndrome
Xeroderma Pigmentosum	Zellweger Syndrome

New Sites - Main » Health » Conditions and Diseases » Genetic Disorders » Organizations

The Ryan Foundation (27th April, 2005) : 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.

Hereditary Hemorrhagic Telangiectasia Foundation International, Inc. (27th April, 2005) : 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 public ...

Australian MPS & Related Diseases Society (27th April, 2005) : 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.

Lysosomal Diseases New Zealand (27th April, 2005) : Information, support and advocacy for families affected by Lysosomal Storage Diseases, a group of rare genetic diseases.

Top Sites - Main » Health » Conditions and Diseases » Genetic Disorders » Organizations

Lysosomal Diseases New Zealand (

) : Information, support and advocacy for families affected by Lysosomal Storage Diseases, a group of rare genetic diseases.

The Ryan Foundation (

) : 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.

Hereditary Hemorrhagic Telangiectasia Foundation International, Inc. (

) : 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 public

Australian MPS & Related Diseases Society (

) : 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.