MetaXearch > / 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 Epidermolysis Bullosa 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 Sirenomelia Smith Lemli Opitz Syndrome Smith-Magenis Syndrome Soto's Syndrome Sturge-Weber Syndrome Thrombocytopenia Absent Radius Syndrome Trichothiodystrophy Turner Syndrome Urea Cycle Usher Syndrome Velo-Cardio-Facial Syndrome Von Hippel-Lindau Waardenburg Syndrome Weaver Syndrome Williams Syndrome Xeroderma Pigmentosum Zellweger Syndrome Dr. Greene's HouseCalls A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. (infos) The UDGD Spot Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis. (infos) Primary Ciliary Dyskinesia Information on a rare congenital disease. (infos) 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. (infos) Genetic and Rare Conditions Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. (infos) 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. (infos) 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. (infos) 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. (infos) Your Genes, Your Health The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed. (infos) 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. (infos) Help build the largest human-edited directory on the web. Submit a Site - Open Directory Project - Become an Editor

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