Monday, February 14, 2011

List of Rare Diseases

what is rare disease?
A rare disease is also known as an orphan disease, is any disease that affects a small percentage of the population. They are extremely very rare and are poorly publicized.

List of rare disease
Addison Disease
Adie Syndrome
Alagille Syndrome
Amyotrophic Lateral Sclerosis
Angelman Syndrome
Angina Pectoris, Variant
Angiolymphoid Hyperplasia with Eosinophilia
Arnold-Chiari Malformation
Arthritis, Juvenile Rheumatoid
Asperger Syndrome
Bardet-Biedl Syndrome
Barrett Esophagus
Beckwith-Wiedemann Syndrome
Behcet Syndrome
Bloom Syndrome
Bowen's Disease
Brachial Plexus Neuropathies
Brown-Sequard Syndrome
Burkitt Lymphoma
Carcinoma 256, Walker
Caroli Disease
Chagas Disease
Charcot-Marie-Tooth Disease
Chediak-Higashi Syndrome
Chiari-Frommel Syndrome
Chondrodysplasia Punctata
Choreatic Disorders
Churg-Strauss Syndrome
Colonic Pseudo-Obstruction
Craniofacial Dysostosis
Creutzfeldt-Jakob Syndrome
Crohn Disease
Cushing Syndrome
De Lange Syndrome
Dementia, Vascular
Dermatitis Herpetiformis
Diffuse Cerebral Sclerosis of Schilder
Duane Retraction Syndrome
Dupuytren's Contracture
Dysautonomia, Familial
Ebstein's Anomaly
Ehlers-Danlos Syndrome
Eisenmenger Complex
Ellis-Van Creveld Syndrome
Epidermal Necrolysis, Toxic
Facial Hemiatrophy
Factor XII Deficiency
Fanconi Anemia
Felty's Syndrome
Fibrous Dysplasia, Polyostotic
Fox-Fordyce Disease
Friedreich Ataxia
Gardner Syndrome
Gaucher Disease
Gerstmann Syndrome
Giant Lymph Node Hyperplasia
Goldenhar Syndrome
Guillain-Barre Syndrome
Hallermann's Syndrome
Hallervorden-Spatz Syndrome
Hamartoma Syndrome, Multiple
Hartnup Disease
Hepatic Vein Thrombosis
Hepatolenticular Degeneration
Hereditary Motor and Sensory Neuropathies
Hippel-Lindau Disease
Hirschsprung Disease
Histiocytic Necrotizing Lymphadenitis
Histiocytosis, Langerhans-Cell
Histiocytosis, Sinus
Hodgkin Disease
Horner Syndrome
Huntington Disease
Hyperostosis, Diffuse Idiopathic Skeletal
Inappropriate ADH Syndrome
Intestinal Polyps
Isaacs Syndrome
Kartagener Syndrome
Kearns-Sayer Syndrome
Keratosis Follicularis
Klippel-Feil Syndrome
Klippel-Trenaunay-Weber Syndrome
Kluver-Bucy Syndrome
Korsakoff Syndrome
Lafora Disease
Lambert-Eaton Myasthenic Syndrome
Landau-Kleffner Syndrome
Langer-Giedion Syndrome
Leigh Disease
Lesch-Nyhan Syndrome
Leukodystrophy, Globoid Cell
Li-Fraumeni Syndrome
Long QT Syndrome
Lymphoma, Mantle-Cell
Machado-Joseph Disease
Mallory-Weiss Syndrome
Marek Disease
Marfan Syndrome
Meckel Diverticulum
Meige Syndrome
Melkersson-Rosenthal Syndrome
Meniere's Disease
Mikulicz' Disease
Miller Fisher Syndrome
Mobius Syndrome
Moyamoya Disease
Mucocutaneous Lymph Node Syndrome
Mullerian Ducts
Munchausen Syndrome by Proxy
Muscular Atrophy, Spinal
Neuroaxonal Dystrophies
Neuromyelitis Optica
Neuronal Ceroid-Lipofuscinoses
Niemann-Pick Diseases
Noonan Syndrome
Osteitis Deformans
Paget's Disease, Mammary
Papillon-Lefevre Disease
Pelizaeus-Merzbacher Disease
Pemphigus, Benign Familial
Penile Induration
Peroxisomal Disorders
Peutz-Jeghers Syndrome
Pierre Robin Syndrome
Pityriasis Lichenoides
Polycystic Ovary Syndrome
Prader-Willi Syndrome
Pulmonary Fibrosis
Pupil Disorders
Raynaud Disease
Reiter Syndrome
Rett Syndrome
Reye Syndrome
Rubinstein-Taybi Syndrome
Sandhoff Disease
Sarcoma, Ewing's
Shwartzman Phenomenon
Shy-Drager Syndrome
Sjogren's Syndrome
Sjogren-Larsson Syndrome
Smith-Lemli-Opitz Syndrome
Spinal Muscular Atrophies of Childhood
Sturge-Weber Syndrome
Sweet's Syndrome
Takayasu's Arteritis
Tangier Disease
Tay-Sachs Disease
Thromboangiitis Obliterans
Tietze's Syndrome
Togaviridae Infections
Tolosa-Hunt Syndrome
Tourette Syndrome
Uveomeningoencephalitic Syndrome
Waardenburg's Syndrome
Waldenstrom Macroglobulinemia
Wegener Granulomatosis
Weil Disease
Werner Syndrome
Williams Syndrome
Wilms Tumor
Wiskott-Aldrich Syndrome
Wolff-Parkinson-White Syndrome
Wolfram Syndrome
Wolman Disease
Zellweger Syndrome
Zollinger-Ellison Syndrome
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