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Genetic Disorders

Information / Diagnosis / Treatment / Prevention
 
                       
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Subtopics:      Genetic Disorders > Aarskog Syndrome          Genetic Disorders > Aase Syndrome
Genetic Disorders > Ablepharon-Macrostomia Syndrome Genetic Disorders > Alagille Syndrome
Genetic Disorders > Alkaptonuria Genetic Disorders > Alpha-1 Antitrypsin Deficiency
Genetic Disorders > Batten Genetic Disorders > Beckwith-Wiedemann Syndrome
Genetic Disorders > Coffin Lowry Syndrome Genetic Disorders > Costello Syndrome
Genetic Disorders > Cowden Syndrome Genetic Disorders > Craniofrontonasal Dysplasia
Genetic Disorders > Crigler-Najjar Syndrome Genetic Disorders > Cystic Fibrosis
Genetic Disorders > DiGeorge Syndrome Genetic Disorders > Down Syndrome
Genetic Disorders > Dubowitz Syndrome Genetic Disorders > Ectodermal Dysplasia
Genetic Disorders > Familial Hypercholesterolemia Genetic Disorders > Fatty Oxidation
Genetic Disorders > Floating-Harbor Syndrome Genetic Disorders > Fragile X Syndrome
Genetic Disorders > Glutaricaciduria Genetic Disorders > Hailey-Hailey Disease
Genetic Disorders > Hemihypertrophy Genetic Disorders > Hemochromatosis
Genetic Disorders > Hereditary Angioedema Genetic Disorders > Hereditary Spastic Paraplegia
Genetic Disorders > Incontinentia Pigmenti Genetic Disorders > Joubert Syndrome
Genetic Disorders > Klinefelter Syndrome Genetic Disorders > Laurence-Moon Syndrome
Genetic Disorders > Lesch-Nyhan Syndrome Genetic Disorders > Lowe Syndrome
Genetic Disorders > Machado-Joseph Genetic Disorders > Mannosidosis
Genetic Disorders > McArdle's Genetic Disorders > Meckel-Gruber Syndrome
Genetic Disorders > Mobius Syndrome Genetic Disorders > Nail Patella Syndrome
Genetic Disorders > Noonan Syndrome Genetic Disorders > Opitz Syndrome
Genetic Disorders > Organizations Genetic Disorders > Pallister-Hall Syndrome
Genetic Disorders > Pallister Killian Mosaic Syndrome Genetic Disorders > Personal Pages
Genetic Disorders > Popliteal Pterygium Syndrome Genetic Disorders > Prader-Willi Syndrome
Genetic Disorders > Propionic Acidemia Genetic Disorders > Proteus Syndrome
Genetic Disorders > Prune Belly Syndrome Genetic Disorders > Pseudoxanthoma Elasticum
Genetic Disorders > Robinow Syndrome Genetic Disorders > Russell Silver Syndrome
Genetic Disorders > Sanfilippo Syndrome Genetic Disorders > Schizencephaly
Genetic Disorders > Shwachman Syndrome Genetic Disorders > Smith-Magenis Syndrome
Genetic Disorders > Smith Lemli Opitz Syndrome Genetic Disorders > Soto's Syndrome
Genetic Disorders > Sturge-Weber Syndrome Genetic Disorders > Thrombocytopenia Absent Radius Syndrome
Genetic Disorders > Turner Syndrome Genetic Disorders > Urea Cycle
Genetic Disorders > Usher Syndrome Genetic Disorders > Velo-Cardio-Facial Syndrome
Genetic Disorders > Von Hippel-Lindau Genetic Disorders > Waardenburg Syndrome
Genetic Disorders > Weaver Syndrome Genetic Disorders > Williams Syndrome
Genetic Disorders > Xeroderma Pigmentosum Genetic Disorders > Zellweger Syndrome
 
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Aicardi Syndrome Albinism
Alopecia Areata Alstrom Syndrome
Angelman Syndrome Apert Syndrome
Arthrogryposis Ataxia
Autism Bardet-Biedl Syndrome
Barth Syndrome Canavan
Celiac Cerebrocostomandibular Syndrome
Charcot-Marie-Tooth Disease Cleidocranial Dysplasia
Cockayne Syndrome Congenital Cardiovascular Disorders
Congenital Heart Disease Congenital Musculoskeletal Disorders
Congenital Neurological Disorders Congenital Pain Insensitivity
Congenital Urological Disorders Cornelia De Lange Syndrome
Cri du Chat Syndrome Cystinosis
Dwarfism Ehlers-Danlos Syndrome
Factor V Leiden Familial Dysautonomia
Familial Erythromelalgia Fanconi Anemia
Friedreich Ataxia Galactosemia
Gaucher's Glycogen Storage Disease Type II
Hallervorden-Spatz Syndrome Hemophilia
Homocystinuria Huntington's
Hydrocephalus Jacobsen Syndrome
Klippel-Feil Syndrome Langer-Giedion Syndrome
Leigh's Leukodystrophy
Lissencephaly Lymphedema
Marfan Syndrome Menkes' Syndrome
Multiple Hereditary Exostoses Muscular Dystrophies
Myotonic Dystrophy Narcolepsy
Neurofibromatosis Niemann-Pick
Osteogenesis Imperfecta Phenylketonuria
Polycystic Kidney Porphyrias
Progeria Refsum's
Retinoblastoma Rett's Syndrome
Rubinstein-Taybi Syndrome Sickle Cell
Spinal Muscular Atrophy Stickler's Syndrome
Support Groups Tay-Sachs
Thalassemia Congenital Anomalies
Rare Disorders Tourette Syndrome
Treacher Collins Syndrome Tuberous Sclerosis
Tyrosinemia VATER Syndrome
WAGR Syndrome Wilson's Disease
new window Open Directory: Genetics Education new window Open Directory: Genetic Testing and Counseling
new window Open Directory: Gene Therapy new window Open Directory: Human Genetics
 
Health Portals:
      new window FamilyDoctor.org Information Sheets: Genetic Testing: What You Should Know
 
 
Health News:
      new window Search millions of published articles for news on Genetic Disorders
The HighBeam™ Research newspaper and magazine archive contains articles from current and back issues of hundreds of publications, including: Modern Medicine, Aging, The Ardell Wellness Report, HealthFacts, Medical Post, Medical Update, Men's Health and the National Women's Health Report.
Note: Subscription required to access the full text of articles.
 
 
MEDLINE/PubMed Database of Research Articles:
     new window Search PubMed Abstracts for "Genetic Disorders"
new window Search PubMed Central Full Text Articles from Life Sciences Journals for "Genetic Disorders"
 
 
Web Directory:
      new window Gene Clinics  [Recommended]   Description: Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. (geneclinics.org)
new window A3243G.com Description: Information about a gene defect which causes a variety of diseases. Find a discussion forum and an newsletter. (a3243g.com)
new window Blepharophimosis Ptosis Epicanthus Inversus Syndrome Description: 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. (freespace.virgin.net)
new window Dr. Greene's HouseCalls Description: A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. (drgreene.com)
new window Genetic and Rare Conditions Description: Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. (kumc.edu)
new window Genetic Disorders: The Links to Diet Description: 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. (ctds.info)
new window IMMD Institute of Medical Molecular Diagnostics Ltd. Description: 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. (immd.de)
new window Primary Ciliary Dyskinesia Description: Information on a rare congenital disease. (p-c-d.org)
new window The Center For Jewish Genetics Disorders Description: A critical effort to provide public and professional education for many of the identified Jewish genetic disorders. Find info on screening and counseling, advocacy, events and community resources. (jewishgeneticscenter.org)
new window The UDGD Spot Description: Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis. (camp-a-roo.com)
new window Washington University in St Louis Description: 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. (siteman.wustl.edu)
new window XLH Network Description: Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets. (xlhnetwork.org)
new window Your Genes, Your Health Description: The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed. (ygyh.org)
 




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Notes: Healthcyclopedia presents health information in the form of websites and articles that encompass conventional medicine and alternative treatments. Under no circumstances can it recommend or endorse a specific therapy or treatment. Symptoms should always be presented to a doctor for tests, diagnosis and possible treatment. Prescription medication should always be taken under a doctor's care. Also pictures on health websites may occasionally be too graphic for younger viewers.