HON - List of Rare Diseases

List of rare diseases: - - - -

Acrocephalosyndactylia	Acrodermatitis
Addison Disease	Adie Syndrome
Alagille Syndrome	Amylose
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
Colorectal Neoplasms, Hereditary Nonpolyposis	Craniofacial Dysostosis
Creutzfeldt-Jakob Syndrome	Crohn Disease
Cushing Syndrome

Dandy-Walker Syndrome	De Lange Syndrome
Dementia, Vascular	Dermatitis Herpetiformis
DiGeorge Syndrome	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
Encephalitis	Enchondromatosis
Epidermal Necrolysis, Toxic

Facial Hemiatrophy	Factor XII Deficiency
Fanconi Anemia	Felty's Syndrome
Fibrous Dysplasia, Polyostotic	Fox-Fordyce Disease
Friedreich Ataxia	Fusobacterium

Gardner Syndrome	Gaucher Disease
Gerstmann Syndrome	Giant Lymph Node Hyperplasia
Glycogen Storage Disease Type I	Glycogen Storage Disease Type II
Glycogen Storage Disease Type IV	Glycogen Storage Disease Type V
Glycogen Storage Disease Type VII	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	Hyperaldosteronism
Hyperostosis, Diffuse Idiopathic Skeletal	Hypopituitarism

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	Mucopolysaccharidosis I
Mucopolysaccharidosis II	Mucopolysaccharidosis III
Mucopolysaccharidosis IV	Mucopolysaccharidosis VI
Mullerian Ducts	Multiple Endocrine Neoplasia Type 1
Munchausen Syndrome by Proxy	Muscular Atrophy, Spinal

Neuroaxonal Dystrophies	Neuromyelitis Optica
Neuronal Ceroid-Lipofuscinoses	Niemann-Pick Diseases
Noonan Syndrome

Optic Atrophies, Hereditary	Osteitis Deformans
Osteochondritis	Osteochondrodysplasias
Osteolysis, Essential

Paget's Disease, Extramammary	Paget's Disease, Mammary
Panniculitis, Nodular Nonsuppurative	Papillon-Lefevre Disease
Paralysis	Pelizaeus-Merzbacher Disease
Pemphigus, Benign Familial	Penile Induration
Pericarditis, Constrictive	Peroxisomal Disorders
Peutz-Jeghers Syndrome	Pick Disease of the Brain
Pierre Robin Syndrome	Pigmentation Disorders
Pityriasis Lichenoides	Polycystic Ovary Syndrome
Polyendocrinopathies, Autoimmune	Prader-Willi Syndrome
Pulmonary Fibrosis	Pupil Disorders

Raynaud Disease	Reiter Syndrome
Rett Syndrome	Reye Syndrome
Rubinstein-Taybi Syndrome

Sandhoff Disease	Sarcoma, Ewing's
Scheuermann's Disease	Shwartzman Phenomenon
Shy-Drager Syndrome	Sjogren's Syndrome
Sjogren-Larsson Syndrome	Smith-Lemli-Opitz Syndrome
Spinal Muscular Atrophies of Childhood	Sturge-Weber Syndrome
Sweating, Gustatory	Sweet's Syndrome

Takayasu's Arteritis	Tangier Disease
Tay-Sachs Disease	Thromboangiitis Obliterans
Thyroiditis, Autoimmune	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

von Willebrand Disease

Others rare diseases or genetic conditions with:

ORPHANET is a database dedicated to information on rare diseases and orphan drugs (available in , , , , and )

National Library of Medicine's web site for consumer information about genetic conditions and the genes or chromosomes responsible for those conditions.
(browse: - - )

HON Foundation is an NGO in Special Consultative Status with the Economic and Social Council of the United Nations

/HONselect/RareDiseases//index.html

Last modified: Jan 7 2009