Genetic Disorders (Conditions and Diseases)

Genetic Disorders further on these related pages:

Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome Acoustic Neuroma@ Adie Syndrome@ Adrenal Hyperplasia@ Adrenoleukodystrophy@ Aicardi Syndrome@ Alagille Syndrome Albinism@ Alkaptonuria Alopecia Areata@ Alpha-1 Antitrypsin Deficiency Alstrom Syndrome@ Angelman Syndrome@ Apert Syndrome@ Arthrogryposis@ Ataxia@ Autism@ Bardet-Biedl Syndrome@ Barth Syndrome@ Batten Beckwith-Wiedemann Syndrome Canavan@ Celiac@ Cerebrocostomandibular Syndrome@ Charcot-Marie-Tooth Disease@ Cleidocranial Dysplasia@ Cockayne Syndrome@ Coffin Lowry Syndrome Congenital Cardiovascular Disorders@ Congenital Heart Disease@ Congenital Musculoskeletal Disorders@ Congenital Neurological Disorders@ Congenital Pain Insensitivity@ Congenital Urological Disorders@ Cornelia De Lange Syndrome@ Costello Syndrome Cowden Syndrome Craniofrontonasal Dysplasia Cri du Chat Syndrome@ Crigler-Najjar Syndrome Cystic Fibrosis Cystinosis@ DiGeorge Syndrome Down Syndrome Dubowitz Syndrome Dwarfism@ Ectodermal Dysplasia Ehlers-Danlos Syndrome@ Factor V Leiden@ Familial Dysautonomia@ Familial Erythromelalgia@ Familial Hypercholesterolemia Fanconi Anemia@ Fatty Oxidation Floating-Harbor Syndrome Fragile X Syndrome Friedreich Ataxia@ Galactosemia@ Gaucher's@ Gene Therapy@ Genetic Testing and Counseling@ Genetics Education@ Glutaricaciduria Glycogen Storage Disease Type II@ Hailey-Hailey Disease Hallervorden-Spatz Syndrome@ Hemihypertrophy Hemochromatosis Hemophilia@ Hereditary Angioedema Hereditary Spastic Paraplegia Homocystinuria@ Human Genetics@ Huntington's@ Hydrocephalus@ Incontinentia Pigmenti Jacobsen Syndrome@

Joubert Syndrome Klinefelter Syndrome Klippel-Feil Syndrome@ Langer-Giedion Syndrome@ Laurence-Moon Syndrome Leigh's@ Lesch-Nyhan Syndrome Leukodystrophy@ Lissencephaly@ Lowe Syndrome Lymphedema@ Machado-Joseph Mannosidosis Marfan Syndrome@ McArdle's Meckel-Gruber Syndrome Menkes' Syndrome@ Mobius Syndrome Multiple Hereditary Exostoses@ Muscular Dystrophies@ Myotonic Dystrophy@ Nail Patella Syndrome Narcolepsy@ Neurofibromatosis@ Niemann-Pick@ Noonan Syndrome Opitz Syndrome Organizations Osteogenesis Imperfecta@ Pallister Killian Mosaic Syndrome Pallister-Hall Syndrome Personal Pages Phenylketonuria@ Polycystic Kidney@ Popliteal Pterygium Syndrome Porphyrias@ Prader-Willi Syndrome Progeria@ Propionic Acidemia Proteus Syndrome Prune Belly Syndrome Pseudoxanthoma Elasticum Refsum's@ Retinoblastoma@ Rett's Syndrome@ Robinow Syndrome Rubinstein-Taybi Syndrome@ Russell Silver Syndrome Sanfilippo Syndrome Schizencephaly Shwachman Syndrome Sickle Cell@ Smith Lemli Opitz Syndrome Smith-Magenis Syndrome Soto's Syndrome Spinal Muscular Atrophy@ Stickler's Syndrome@ Sturge-Weber Syndrome Support Groups@ Tay-Sachs@ Thalassemia@ Thrombocytopenia Absent Radius Syndrome Tourette Syndrome@ Treacher Collins Syndrome@ Tuberous Sclerosis@ Turner Syndrome Tyrosinemia@ Urea Cycle Usher Syndrome VATER Syndrome@ Velo-Cardio-Facial Syndrome Von Hippel-Lindau WAGR Syndrome@ Waardenburg Syndrome Weaver Syndrome Williams Syndrome Wilson's Disease@ Xeroderma Pigmentosum Zellweger Syndrome

Top/Health/Conditions and Diseases/Congenital Anomalies Top/Health/Conditions and Diseases/Rare Disorders

Genetic Disorders Sites:

The UDGD Spot The UDGD Spot: Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis. (Genetic Disorders) http://www.camp-a-roo.com/UDGD/ Dr. Greene's HouseCalls Dr. Greene's HouseCalls: A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. (Genetic Disorders) http://www.drgreene.com/html/21614.html Genetic Disorders: The Links to Diet 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. (Genetic Disorders) http://www.ctds.info/genetic_disorders.html Primary Ciliary Dyskinesia Primary Ciliary Dyskinesia: Information on a rare congenital disease. (Genetic Disorders) http://www.p-c-d.org/en/ Washington University in St Louis 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. (Genetic Disorders) http://www.siteman.wustl.edu/physician/clinical_trials/non_therapeutic_1736_detail.shtml Gene Clinics 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 Disorders) http://www.geneclinics.org Your Genes, Your Health Your Genes, Your Health: The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed. (Genetic Disorders) http://www.ygyh.org Genetic and Rare Conditions 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. (Genetic Disorders) http://www.kumc.edu/gec/support/ IMMD Institute of Medical Molecular Diagnostics Ltd. 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. (Genetic Disorders) http://www.immd.de/ Blepharophimosis Ptosis Epicanthus Inversus Syndrome 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. (Genetic Disorders) http://freespace.virgin.net/andy.bowles/ XLH Network 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) http://www.xlhnetwork.org