Diseases : Genetic Disorders : BioSpace : CCIS : Genetic Disorders

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