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Rare Disorders

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Subtopics:      Rare Disorders > Agnosia          Rare Disorders > Aicardi Syndrome
Rare Disorders > Alstrom Syndrome Rare Disorders > Barth Syndrome
Rare Disorders > Cerebrocostomandibular Syndrome Rare Disorders > Cleidocranial Dysplasia
Rare Disorders > Cystinosis Rare Disorders > Degos
Rare Disorders > Erythromelalgia Rare Disorders > Jacobsen Syndrome
Rare Disorders > Melorheostosis Rare Disorders > Moyamoya
Rare Disorders > Ollier Disease Rare Disorders > Pemphigoid
Rare Disorders > Pemphigus Rare Disorders > Phenylketonuria
Rare Disorders > Pierre Robin Syndrome Rare Disorders > Progeria
Rare Disorders > Rubinstein-Taybi Syndrome Rare Disorders > Tyrosinemia
Rare Disorders > VATER Syndrome Rare Disorders > Wegener's Granulomatosis
 
Related Topics:      Aarskog Syndrome          Aase Syndrome
Abetalipoproteinemia Ablepharon-Macrostomia Syndrome
Adie Syndrome Adrenoleukodystrophy
Alagille Syndrome Alternating Hemiplegia
Apert Syndrome Arthrogryposis
Ataxia Bardet-Biedl Syndrome
Behcet's Syndrome Blastomycosis
Botulism Celiac
Charcot-Marie-Tooth Disease Cockayne Syndrome
Coffin Lowry Syndrome Cornelia De Lange Syndrome
Corticobasal Degeneration Costello Syndrome
Craniofrontonasal Dysplasia Crigler-Najjar Syndrome
Cri du Chat Syndrome Cyclic Vomiting Syndrome
Dandy Walker Syndrome Dercum Disease
DiGeorge Syndrome Dubowitz Syndrome
Dystonia Ehlers-Danlos Syndrome
Fabry's Familial Dysautonomia
Fanconi Anemia Floating-Harbor Syndrome
Friedreich Ataxia Galactosemia
Gaucher's Gerstmann Syndrome
Glutaricaciduria Guillain-Barre Syndrome
Gustatory Sweating Hallervorden-Spatz Syndrome
Hemihypertrophy Hemophilia
Hereditary Angioedema Hidradenitis Suppurativa
Homocystinuria Horner Syndrome
Huntington's Hydrocephalus
Incontinentia Pigmenti Isaacs Syndrome
Joubert Syndrome Kearns Sayre Syndrome
Kernicterus Klippel-Feil Syndrome
Kluver-Bucy Syndrome Laurence-Moon Syndrome
Leigh's Lesch-Nyhan Syndrome
Lissencephaly Lowe Syndrome
Madelung's Mannosidosis
Marfan Syndrome Mastocytosis
Meige Syndrome Mobius Syndrome
Multiple Hereditary Exostoses Myotonic Dystrophy
Nail Patella Syndrome Narcolepsy
Neurofibromatosis Neuroleptic Malignant Syndrome
Niemann-Pick Noonan Syndrome
Olivopontocerebellar Atrophy Opitz Syndrome
Osteogenesis Imperfecta Pallister-Hall Syndrome
Pallister Killian Mosaic Syndrome Pick Disease of the Brain
POEMS Syndrome Porencephaly
Porphyrias Prader-Willi Syndrome
Propionic Acidemia Proteus Syndrome
Prune Belly Syndrome Pseudoxanthoma Elasticum
Refsum's Retinoblastoma
Rett's Syndrome Rickets
Robinow Syndrome Russell Silver Syndrome
Sanfilippo Syndrome Schizencephaly
Shwachman Syndrome Smith-Magenis Syndrome
Smith Lemli Opitz Syndrome Spina Bifida
Stickler's Syndrome Stiff-Person Syndrome
Sturge-Weber Syndrome Subacute Sclerosing Panencephalitis
Tangier Tay-Sachs
Thalassemia Thrombocytopenia Absent Radius Syndrome
Genetic Disorders Tourette Syndrome
Treacher Collins Syndrome Tuberous Sclerosis
Turner Syndrome Usher Syndrome
Velo-Cardio-Facial Syndrome Waardenburg Syndrome
WAGR Syndrome Weaver Syndrome
Williams Syndrome Wilson's Disease
Xeroderma Pigmentosum Zellweger Syndrome
Zollinger-Ellison Syndrome   
 
Message Boards and Online Support Groups:
      new window iVillage.com - The Women's Network: Rare Diseases & Disorders
 
 
Health News:
      new window Search millions of published articles for news on Rare 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 "Rare Disorders"
new window Search PubMed Central Full Text Articles from Life Sciences Journals for "Rare Disorders"
 
 
Web Directory:
      new window National Organization for Rare Disorders, Inc.  [Recommended]   Description: Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching. (rarediseases.org)
new window Cherubs Description: A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. (cherubs-cdh.org)
new window Contact a Family Description: Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. (cafamily.org.uk)
new window Fibrosing Mediastinitis Description: The least common, but most severe, late complication of histoplasmosis. Educational and research information. Includes interviews, patient stories, and a community forum. (fibrosingmediastinitis.com)
new window Fibrous Dysplasia Support Online Description: For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. (members.cox.net)
new window Human Growth Foundation Description: Information about growth-related disorders through education, research, and advocacy. Member driven organization. (hgfound.org)
new window Information Centre for Rare Diseases and Orphan Drugs Description: Offers an Internet portal. Includes news, forums, rare disease and orphan drug info and registration forms (raredis.org)
new window International Rare Disease Support Network Description: A community providing more than a 1000 different links to support groups for the people of all nations. (raredisorders.com)
new window Kindler Syndrome Description: An article and case study of this rare disease. Includes links. (digilander.libero.it)
new window Lymphangiomatosis and Gorham's Vanishing Bone Disease Description: Provides general information and a personal account, including pictures and X-rays. Also offers patient contact and an email discussion group. (gorhams.dk)
new window Mascot McCune Allbright Syndrome Communication Online Town Description: Collects all the brand new studies in McCune syndrome and perform a FAQ session to explain what the disease is. It is a sharing experience place for ill people. (mascot.altervista.org)
new window Nomid /Cinca Description: Resource for parents and patients suffering from Neonatal Onset Multi-inflammatory Disease Chronic, or Infantile, Neurologic, Cutaneous and Articular syndrome. Site maintained by patients, parents and friends for their counterparts worldwide. Email support group at eGroups. (pweb.netcom.com)
new window Office of Rare Diseases Description: Information on more than 6000 rare diseases, including current research, publications from scientific and medical journals, completed research, ongoing studies, and patient support groups. (rarediseases.info.nih.gov)
new window Tetrahydrobiopterin Description: Information on structure, biosynthesis and pathophysiology of BH4 and tetrahydrobiopterin deficiency. (bh4.org)
 




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