Informaţii despre

Nume Scoliosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Scoliosis, unspecified
Clasificare anatomică Malacards Boli osoase
Boli din aceeaşi familie Infantile Scoliosis

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Boli A-Z Aarskog-Scott Syndrome Absent Patella Achalasia Achondroplasia Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Adie Pupil Aging Aicardi Syndrome Aland Island Eye Disease Alexander Disease Alexithymia Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Aortic Coarctation Arachnoid Cysts Arachnoiditis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 9 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthropathy, Progressive Pseudorheumatoid, of Childhood Asherman's Syndrome Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Back Pain Beckwith-Wiedemann Syndrome Beukes Hip Dysplasia Blau Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Development Disease Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Structure Disease Brachydactyly Brachydactyly, Type A1 Brittle Bone Disorder Buruli Ulcer Cataract Cavernous Hemangioma Central Retinal Artery Occlusion Cerebral Atrophy Cerebral Palsy Cerebritis Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease Chiari Malformation Chiari Malformation Type I Chromosomal Triplication Chromosome 14q Deletion Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 2q35 Duplication Syndrome Chromosome 3q Duplication Chronic Inflammatory Demyelinating Polyneuropathy Chronic Recurrent Multifocal Osteomyelitis Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Collagen Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Congenital Myasthenic Syndrome Congenital Ptosis Congenital Torticollis Conjugate Gaze Palsy Cor Triatriatum Costello Syndrome Cri-Du-Chat Syndrome Cutis Laxa Cystic Fibrosis Dandy-Walker Syndrome Degenerative Disc Disease Demyelinating Polyneuropathy Desmoid Tumor Diastematomyelia Diastrophic Dysplasia Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation Distal Arthrogryposis Duane Retraction Syndrome 1 Dubowitz Syndrome Dwarfism Dysautonomia Dysostosis Dystonia Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Eosinophilia, Familial Ependymoma Epidural Abscess Esophageal Atresia Esotropia Exostoses, Multiple, Type Ii Exostosis Factor Vii Deficiency Fanconi Anemia, Complementation Group E Fibrodysplasia Ossificans Progressiva Fibromatosis Fibrous Dysplasia Focal Dystonia Frontometaphyseal Dysplasia Galactosialidosis Ganglioneuroblastoma Ganglioneuroma Gastroesophageal Reflux Gigantism Gigantomastia Gilbert Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioma Glucose Transporter Type 1 Deficiency Syndrome Growth Hormone Deficiency Hemangioendothelioma Hemangioma Hemi 3 Syndrome Hemihyperplasia, Isolated Hemiplegia Hemophilia Hemophilia B Hepatic Adenomas, Familial High Bone Mass Osteogenesis Imperfecta Hip Subluxation Horizontal Gaze Palsy with Progressive Scoliosis Hydrocephalus Hydromyelia Hyperostosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypotonia Idiopathic Scoliosis Idiopathic Syringomyelia Infantile Scoliosis Insulin-Like Growth Factor I Intracranial Hypotension Juvenile Primary Osteoporosis Juvenile Spinal Muscular Atrophy Kaposiform Hemangioendothelioma Kaposi Sarcoma Kartagener Syndrome Keratoconus Klippel-Feil Syndrome Klippel-Trenaunay-Weber Syndrome Lacrimoauriculodentodigital Syndrome Larsen-Like Syndrome Larsen Syndrome Lathyrism Lentigines Lipomatosis Loeys-Dietz Syndrome Lung Disease Lymphocele Macs Syndrome Malignant Hyperthermia Malignant Hyperthermia Susceptibility Malignant Peripheral Nerve Sheath Tumor Maple Syrup Urine Disease Marden-Walker Syndrome Marfan Syndrome Mast Cell Activation Syndrome Mccune-Albright Syndrome Meningocele Menkes Disease Microcephaly Motion Sickness Multiminicore Disease Multiple Epiphyseal Dysplasia Multiple Pterygium Syndrome, Escobar Variant Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne Type Myelitis Myelomeningocele Myopathy Myopia Myopia 6 Myosin Storage Myopathy Myotonia Myotonia Congenita Myxopapillary Ependymoma Neuroblastoma Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronitis Neutrophilic Dermatosis, Acute Febrile Nipples, Supernumerary Ochronosis Oliver-Mcfarlane Syndrome Omphalocele Optic Pathway Glioma Osgood-Schlatter's Disease Osteoblastoma Osteochondrodysplasia Osteochondroma Osteochondrosis Osteogenesis Imperfecta, Type I Osteogenesis Imperfecta, Type Ii Osteogenesis Imperfecta, Type Vii Osteogenesis Imperfecta, Type Viii Osteoid Osteoma Osteomyelitis Osteopetrosis Pallister-Hall Syndrome Pectus Carinatum Pectus Excavatum Pentalogy of Cantrell Phacomatosis Pigmentokeratotica Plagiocephaly Plexiform Neurofibroma Plexopathy Polyneuropathy Posterior Column Ataxia Prader-Willi Syndrome Proteus Syndrome Proximal Spinal Muscular Atrophy Prune Belly Syndrome Ptosis Quadriplegia Radial Hemimelia Radiculopathy Radioulnar Synostosis Radioulnar Synostosis-Microcephaly-Scoliosis Syndrome Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation Retinal Artery Occlusion Retinitis Rett Syndrome Sacrococcygeal Teratoma Salt and Pepper Developmental Regression Syndrome Sarcoma Scar Contracture Scheuermann Disease Schinzel Giedion Syndrome Scleroderma, Familial Progressive Scoliosis, Isolated 1 Scoliosis, Isolated 2 Scott Syndrome Seizures, Benign Familial Neonatal, 1 Situs Inversus Skeletal Dysplasias Skin Disease Slipped Capital Femoral Epiphysis Smith-Magenis Syndrome Sotos Syndrome 1 Spastic Cerebral Palsy Spasticity Spastic Quadriplegia Spina Bifida Occulta Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Astrocytoma Spinal Cord Injury Spinal Disease Spinal Muscular Atrophy Spinal Muscular Atrophy, Type Ii Spinal Stenosis Spitz Nevus Split Spinal Cord Malformation Spondylocarpotarsal Synostosis Syndrome Spondylocostal Dysostosis 1, Autosomal Recessive Spondylocostal Dysostosis 3, Autosomal Recessive Spondylocostal Dysostosis, Autosomal Recessive Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondyloepiphyseal Dysplasia Congenita Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondylolisthesis Spondylolysis Spondylosis Steel Syndrome Stuve-Wiedemann Syndrome Superior Mesenteric Artery Syndrome Supranuclear Ocular Palsy Synostosis Synovial Chondromatosis Synpolydactyly Syringohydromyelia Syringomyelia Talipes Equinovarus Teratoma Tethered Cord Syndrome Tetralogy of Fallot Three M Syndrome 1 Thrombosis Tonsillitis Tooth Disease Torticollis Tracheobronchomalacia Tracheoesophageal Fistula Tremor Turner Syndrome Ulnar Hypoplasia Urinary Tract Obstruction Vacterl Association Ventricular Septal Defect Weber Syndrome Wildervanck Syndrome Williams-Beuren Syndrome