Rare Disorders
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Health
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Conditions and Diseases
: Rare Disorders
(124)
Aarskog Syndrome
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(4)
Aase Syndrome
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(3)
Abetalipoproteinemia
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(1)
Ablepharon-Macrostomia Syndrome
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(4)
Adie Syndrome
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(3)
Adrenoleukodystrophy
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(6)
Agnosia
(7)
Aicardi Syndrome
(7)
Alagille Syndrome
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(7)
Alström Syndrome
(3)
Alternating Hemiplegia
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(3)
Apert Syndrome
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(9)
Arthrogryposis
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(49)
Ataxia
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(8)
Bardet-Biedl Syndrome
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(3)
Barth Syndrome
(3)
Behcet's Syndrome
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(9)
Blastomycosis
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(5)
Botulism
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(16)
Celiac
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(56)
Cerebrocostomandibular Syndrome
(2)
Charcot-Marie-Tooth Disease
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(7)
Cleidocranial Dysplasia
(3)
Cockayne Syndrome
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(3)
Coffin Lowry Syndrome
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(4)
Cornelia De Lange Syndrome
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(4)
Corticobasal Degeneration
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(3)
Costello Syndrome
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(2)
Craniofrontonasal Dysplasia
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(3)
Cri du Chat Syndrome
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(4)
Crigler-Najjar Syndrome
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(7)
Cyclic Vomiting Syndrome
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(9)
Cystinosis
(8)
Dandy Walker Syndrome
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(3)
Degos
(4)
Dercum Disease
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(13)
DiGeorge Syndrome
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(4)
Dubowitz Syndrome
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(3)
Dystonia
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(25)
Ehlers-Danlos Syndrome
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(27)
Erythromelalgia
(3)
Fabry's
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(9)
Familial Dysautonomia
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(8)
Fanconi Anemia
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(12)
Fibrodysplasia Ossificans Progressiva
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(3)
Floating-Harbor Syndrome
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(4)
Friedreich Ataxia
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(12)
Galactosemia
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(5)
Gaucher's
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(13)
Gerstmann Syndrome
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(3)
Glutaricaciduria
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(3)
Guillain-Barre Syndrome
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(12)
Gustatory Sweating
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(2)
Hallervorden-Spatz Syndrome
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(3)
Hemihypertrophy
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(3)
Hemophilia
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(26)
Hereditary Angioedema
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(6)
Hidradenitis Suppurativa
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(12)
Homocystinuria
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(2)
Horner Syndrome
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(2)
Huntington's
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(25)
Hydrocephalus
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(42)
Idiopathic Pulmonary Hemosiderosis
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(3)
Incontinentia Pigmenti
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(7)
Isaacs Syndrome
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(2)
Jacobsen Syndrome
(0)
Joubert Syndrome
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(7)
Kearns Sayre Syndrome
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(2)
Kernicterus
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(1)
Klippel-Feil Syndrome
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(6)
Kluver-Bucy Syndrome
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(2)
Laurence-Moon Syndrome
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(3)
Leigh's
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(4)
Lesch-Nyhan Syndrome
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(1)
Lissencephaly
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(5)
Lowe Syndrome
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(2)
Madelung's
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(8)
Mannosidosis
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(2)
Marfan Syndrome
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(24)
Mastocytosis
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(371)
Meige Syndrome
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(3)
Melorheostosis
(1)
Mobius Syndrome
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(5)
Moyamoya
(7)
Multiple Hereditary Exostoses
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(6)
Myotonic Dystrophy
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(4)
Nail Patella Syndrome
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(4)
Narcolepsy
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(18)
Neurofibromatosis
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(15)
Neuroleptic Malignant Syndrome
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(5)
Niemann-Pick
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(4)
Noonan Syndrome
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(8)
Olivopontocerebellar Atrophy
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(3)
Ollier Disease
(1)
Opitz Syndrome
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(4)
Osteogenesis Imperfecta
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(14)
Pallister Killian Mosaic Syndrome
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(9)
Pallister-Hall Syndrome
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(3)
Pemphigoid
(1)
Pemphigus
(5)
Phenylketonuria
(9)
Pick Disease of the Brain
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(4)
Pierre Robin Syndrome
(4)
POEMS Syndrome
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(2)
Porencephaly
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(4)
Porphyrias
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(13)
Prader-Willi Syndrome
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(9)
Progeria
(10)
Propionic Acidemia
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(5)
Proteus Syndrome
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(5)
Prune Belly Syndrome
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(2)
Pseudoxanthoma Elasticum
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(5)
Refsum's
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(3)
Retinoblastoma
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(24)
Rett's Syndrome
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(19)
Rickets
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(10)
Robinow Syndrome
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(4)
Rubinstein-Taybi Syndrome
(6)
Russell Silver Syndrome
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(3)
Sanfilippo Syndrome
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(7)
Schizencephaly
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(1)
Shwachman Syndrome
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(7)
Smith Lemli Opitz Syndrome
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(3)
Smith-Magenis Syndrome
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(3)
Spina Bifida
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(35)
Stickler's Syndrome
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(3)
Stiff-Person Syndrome
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(4)
Sturge-Weber Syndrome
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(4)
Subacute Sclerosing Panencephalitis
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(2)
Tangier
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(2)
Tay-Sachs
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(4)
Thalassemia
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(21)
Thrombocytopenia Absent Radius Syndrome
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(3)
Tourette Syndrome
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(56)
Treacher Collins Syndrome
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(4)
Trichothiodystrophy
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(10)
Triploidy
(3)
Tuberous Sclerosis
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(11)
Turner Syndrome
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(13)
Tyrosinemia
(2)
Usher Syndrome
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(2)
VACTERL Association
(17)
Velo-Cardio-Facial Syndrome
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(5)
Waardenburg Syndrome
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(2)
WAGR Syndrome
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(3)
Weaver Syndrome
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(2)
Wegener's Granulomatosis
(9)
Williams Syndrome
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(17)
Wilson's Disease
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(11)
Xeroderma Pigmentosum
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(6)
Zellweger Syndrome
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(7)
Zollinger-Ellison Syndrome
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(4)
See also:
Health: Conditions and Diseases: Genetic Disorders
(678)
This category in other languages:
French
(37)
Italian
(33)
Japanese
(15)
National Organization for Rare Disorders, Inc.
- 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.
Cherubs
- A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia.
Contact a Family
- Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK.
European Organisation for Rare Diseases
- Alliance of patient associations dedicated to improving the quality of life of all people living with rare diseases in Europe.
Fibrous Dysplasia Support Online
- For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism.
Human Growth Foundation
- Information about growth-related disorders through education, research, and advocacy. Member driven organization.
Information Centre for Rare Diseases and Orphan Drugs
- Offers an Internet portal. Includes news, forums, rare disease and orphan drug information and registration forms
Kindler Syndrome
- An article and case study of this rare disease. Includes links.
Office of Rare Diseases
- Information on more than 6000 rare diseases, including current research, publications from scientific and medical journals, completed research, ongoing studies, and patient support groups.
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