NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases
About NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases
The mission of the National Institute of Arthritis and Musculoskeletal and Skin Diseases is to support research into the causes, treatment, and prevention of arthritis and musculoskeletal and skin diseases; the training of basic and clinical scientists to carry out this research; and the dissemination of information on research progress in these diseases.
Related Rare Diseases:
- Chanarin-Dorfman Syndrome
- Síndrome trico-dento-óseo
- Síndrome Periódico Asociado al Receptor del Factor de Necrosis Tumoral (TRAPS)
- Enfermedad de Mucha Habermann
- Síndrome de Binder
- Síndrome de Primrose
- Fibrodisplasia osificante progresiva
- Heteroplasia ósea progresiva
- Síndrome trico-rino-falángico tipo 1
- Síndrome trico-rino-falángico tipo 2
- Mastocitosis
- Artrogriposis Múltiple Congénita
- Congenital Myasthenic Syndromes
- Nevus Sebaceus Syndrome
- Pityriasis Rosea
- Hailey-Hailey Disease
- Adult-Onset Still’s Disease
- Autoimmune Blistering Diseases
- Schnitzler Syndrome
- Congenital Muscular Dystrophy
- Pseudoachondroplasia
- Hyper IgM Syndromes
- Schinzel Syndrome
- Setleis Syndrome
- Acromesomelic Dysplasia
- Haim-Munk Syndrome
- Meleda Disease
- Trichorhinophalangeal Syndrome Type III
- PMM2-CDG
- Leri Pleonosteosis
- IRF6-Related Disorders
- Meier-Gorlin Syndrome
- Laband Syndrome
- Papillon Lefèvre Syndrome
- Fountain Syndrome
- Schwartz Jampel Syndrome
- De Sanctis Cacchione Syndrome
- Pycnodysostosis
- Cutis Marmorata Telangiectatica Congenita
- De Barsy Syndrome
- Hypomelanosis of Ito
- Hereditary Multiple Osteochondromas
- Campomelic Syndrome
- Sprengel Deformity
- Fox Fordyce Disease
- Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate
- Floating Harbor Syndrome
- Focal Dermal Hypoplasia
- Oculo-Dento-Digital Dysplasia
- Aplasia Cutis Congenita
- Grover’s Disease
- Jansen Type Metaphyseal Chondrodysplasia
- LADD syndrome
- Keratitis Ichthyosis Deafness Syndrome
- Hyperostosis Frontalis Interna
- Epidermal Nevus Syndromes
- Fibrous Dysplasia
- Diffuse Idiopathic Skeletal Hyperostosis
- DOORS Syndrome
- Hypohidrotic Ectodermal Dysplasia
- Osteonecrosis
- Osteomyelitis
- Robinow Syndrome
- Dupuytren’s Contracture
- Gianotti Crosti Syndrome
- Mucous Membrane Pemphigoid
- Tietze Syndrome
- Acrodysostosis
- Bowen Disease
- Blue Rubber Bleb Nevus syndrome
- Kienböck Disease
- Hypochondroplasia
- Peeling Skin Syndrome
- Nail Patella Syndrome
- Legg Calvé Perthes Disease
- Relapsing Polychondritis
- Ichthyosis
- Erythrokeratodermia with Ataxia
- Erythrokeratoderma
- Sjögren-Larsson Syndrome
- Lamellar Ichthyosis
- Ichthyosis Vulgaris
- Holt Oram Syndrome
- Gordon Syndrome
- Larsen Syndrome
- Diastrophic Dysplasia
- Prune Belly Syndrome
- Rubinstein-Taybi Syndrome
- Granuloma Annulare
- Lymphocytic Infiltrate of Jessner
- Alopecia Areata
- Poland Syndrome
- Maffucci Syndrome
- Coffin Lowry Syndrome
- Sweet Syndrome
- Stickler Syndrome
- Incontinentia Pigmenti
- Myotonia Congenita
- Shwachman Diamond Syndrome
- Conradi Hünermann Syndrome
- Hidradenitis Suppurativa
- Myotonic Dystrophy
- Osteopetrosis
- Felty Syndrome
- Xeroderma Pigmentosum
- Ollier Disease
- Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
- Erythema Multiforme
- Fibromyalgia
- Polymyalgia Rheumatica
- Pseudoxanthoma Elasticum
- Lichen Sclerosus
- Lichen Planus
- Dermatitis Herpetiformis
- McCune-Albright Syndrome
- Cutis Laxa
- Three M Syndrome
- Ankylosing Spondylitis
- Acanthosis Nigricans
- Reactive Arthritis
- WAS Related Disorders
- Scleroderma
- Bullous Pemphigoid
- Lupus
- Sjögren Syndrome
- Queratosis folicular
- Síndrome de Marfan
- Síndromes de Ehlers-Danlos
- Síndrome de Hermansky Pudlak
- Acondroplasia
- Síndrome de Behçet
- Eritromelalgia
- Síndrome de la piel escaldada por estafilococos
- Síndrome de Klippel-Feil
- Displasia cleidocraneal
- Síndrome de Rothmund-Thomson
- Pénfigo y penfigoide
- Enfermedad de Erdheim-Chester
- Displasia epifisaria hemimélica
- Síndrome de Proteus
- Ictiosis epidermolítica
- Síndrome de Simpson-Golabi-Behmel
- Pioderma gangrenoso
- Osteogénesis imperfecta
- Paniculitis nodular idiopática
- Eritema queratolítico invernal
- Malformación de mano dividida/pie dividido
- Gangrena de Fournier
- Síndrome de abléfaron-macrostomía
- Síndrome de Aarskog
- Síndrome de Winchester
- Espectro osteólisis multicéntrica-nodulosis-artropatía
- Síndrome de Hajdu Cheney
- Síndrome oculocerebral con hipopigmentación
- Síndrome de tortuosidad arterial