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
- Congenital Myasthenic Syndromes
- Arterial Tortuosity Syndrome
- Nevus Sebaceus Syndrome
- Pityriasis Rosea
- Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
- Hailey-Hailey Disease
- Adult-Onset Still’s Disease
- Autoimmune Blistering Diseases
- Schnitzler Syndrome
- Congenital Muscular Dystrophy
- Fournier Gangrene
- Pseudoachondroplasia
- Hyper IgM Syndromes
- Schinzel Syndrome
- Ablepharon-Macrostomia Syndrome
- Setleis Syndrome
- Acromesomelic Dysplasia
- Haim-Munk Syndrome
- Meleda Disease
- Trichorhinophalangeal Syndrome Type III
- Trichorhinophalangeal Syndrome Type II
- PMM2-CDG
- Leri Pleonosteosis
- IRF6-Related Disorders
- Meier-Gorlin Syndrome
- Laband Syndrome
- Papillon Lefèvre Syndrome
- Oculocerebral Syndrome with Hypopigmentation
- Fountain Syndrome
- Schwartz Jampel Syndrome
- Progressive Osseous Heteroplasia
- De Sanctis Cacchione Syndrome
- Pycnodysostosis
- Cutis Marmorata Telangiectatica Congenita
- Simpson-Golabi-Behmel Syndrome
- De Barsy Syndrome
- Hypomelanosis of Ito
- Hereditary Multiple Osteochondromas
- Campomelic Syndrome
- Cleidocranial Dysplasia
- Binder Type Nasomaxillary Dysplasia
- Hermansky Pudlak Syndrome
- Erdheim Chester Disease
- Sprengel Deformity
- Fox Fordyce Disease
- Winchester Syndrome
- 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
- Hajdu Cheney Syndrome
- Hyperostosis Frontalis Interna
- Epidermal Nevus Syndromes
- Fibrous Dysplasia / McCune-Albright Syndrome
- Diffuse Idiopathic Skeletal Hyperostosis
- DOORS Syndrome
- Hypohidrotic Ectodermal Dysplasia
- Osteonecrosis
- Mucha Habermann Disease
- Osteomyelitis
- Trichorhinophalangeal Syndrome Type I
- Robinow Syndrome
- Rothmund-Thomson Syndrome
- Split Hand/Split Foot Malformation
- Dupuytren’s Contracture
- Gianotti Crosti Syndrome
- Klippel-Feil Syndrome
- Mucous Membrane Pemphigoid
- Tietze Syndrome
- Aarskog Syndrome
- Acrodysostosis
- Bowen Disease
- Blue Rubber Bleb Nevus syndrome
- Kienböck Disease
- Hypochondroplasia
- Proteus Syndrome
- Peeling Skin Syndrome
- Dysplasia Epiphysealis Hemimelica
- Pyoderma Gangrenosum
- Nail Patella Syndrome
- Legg Calvé Perthes Disease
- Relapsing Polychondritis
- Ichthyosis
- Keratolytic Winter Erythema
- Erythrokeratodermia with Ataxia
- Erythrokeratoderma
- Sjögren-Larsson Syndrome
- Lamellar Ichthyosis
- Ichthyosis Vulgaris
- Holt Oram Syndrome
- Gordon Syndrome
- Larsen Syndrome
- Keratosis Follicularis
- Diastrophic Dysplasia
- Prune Belly Syndrome
- Epidermolytic Ichthyosis
- Rubinstein-Taybi Syndrome
- Granuloma Annulare
- Lymphocytic Infiltrate of Jessner
- Alopecia Areata
- Mastocytosis
- Poland Syndrome
- Maffucci Syndrome
- Coffin Lowry Syndrome
- Sweet Syndrome
- Stickler Syndrome
- Staphylococcal Scalded Skin Syndrome
- Incontinentia Pigmenti
- Tricho Dento Osseous Syndrome
- Myotonia Congenita
- Shwachman Diamond Syndrome
- Fibrodysplasia Ossificans Progressiva
- Conradi Hünermann Syndrome
- Hidradenitis Suppurativa
- Myotonic Dystrophy
- Osteopetrosis
- Felty Syndrome
- Xeroderma Pigmentosum
- Ollier Disease
- Idiopathic Nodular Panniculitis
- Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
- Erythema Multiforme
- Fibromyalgia
- Polymyalgia Rheumatica
- Pseudoxanthoma Elasticum
- Lichen Sclerosus
- Erythromelalgia
- Ehlers Danlos Syndrome
- Lichen Planus
- Arthrogryposis Multiplex Congenita
- Dermatitis Herpetiformis
- McCune-Albright Syndrome
- Cutis Laxa
- Three M Syndrome
- Ankylosing Spondylitis
- Acanthosis Nigricans
- Reactive Arthritis
- WAS-Related Disorders
- Scleroderma
- Bullous Pemphigoid
- Pemphigus and Pemphigoid
- Lupus
- Marfan Syndrome
- Osteogenesis Imperfecta
- Sjögren Syndrome
- Behçet’s 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
- Multicentric Osteolysis Nodulosis and Arthropathy Spectrum
- Espectro osteólisis multicéntrica-nodulosis-artropatía
- Síndrome de Hajdu Cheney
- Síndrome oculocerebral con hipopigmentación
- Síndrome de tortuosidad arterial
- Primrose Syndrome