Genetic Disorders Home>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-Hall Syndrome    Pallister Killian Mosaic 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-Magenis Syndrome    Smith Lemli Opitz 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      Web Pages Dr. Greene's HouseCalls A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. The UDGD Spot Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis. Primary Ciliary Dyskinesia Information on a rare congenital disease. Gene Clinics Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. Genetic and Rare Conditions Site Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. XLH Network Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets. Genetic Disorders: The Links to Diet Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis. Washington University in St Louis Family resource for individuals with Papillon Lefevre, Haim-Munk Syndrome and Prepubertal Periodontis. Interested families may participate in a registry dedicated to learning about the natural history of these three conditions. Your Genes, Your Health The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed. Blepharophimosis Ptosis Epicanthus Inversus Syndrome The BPEI (BPES) Family Network encourages people to get in touch with each other, share information and ask questions. Explanation of this rare eye disorder. IMMD Institute of Medical Molecular Diagnostics Ltd. The IMMD is a genetic testing laboratory located in Germany. Provides genetic tests for hereditary breast cancer, various cardiovascular diseases or diseases with onset in childhood.