Informaţii despre

Nume Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Spondyloepiphyseal dysplasia
Clasificare anatomică Malacards Boli osoase

Vezi şi

Boli A-Z Achondrogenesis Achondrogenesis, Type Ia Achondrogenesis, Type Ii Achondroplasia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Andersen Cardiodysrhythmic Periodic Paralysis Aniridia 1 Anorexia Nervosa 1 Arterial Tortuosity Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asphyxiating Thoracic Dystrophy Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atlantoaxial Subluxation Blood Group--Ahonen Blood Group, I System Bone Deterioration Disease Bone Development Disease Brachydactyly Brachyolmia Cartilage Disease Cataract Cavitary Optic Disc Anomalies Cervicitis Clubfoot Codas Syndrome Collagenopathy, Types Ii and Xi Diastrophic Dysplasia Dwarfism Dysostosis Epiphysiolysis of the Hip Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Helix Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypochondrogenesis Intervertebral Disc Disease Juvenile Rheumatoid Arthritis Kniest Dysplasia Larsen Syndrome Leber Congenital Amaurosis 4 Leber Hereditary Optic Neuropathy Lymphopenia Mast Cell Activation Syndrome Metaphyseal Chondrodysplasia, Jansen Type Mucopolysaccharidoses Mucopolysaccharidosis Iv Mucopolysaccharidosis-Plus Syndrome Multiple Epiphyseal Dysplasia Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects Nephrotic Syndrome Neuropathy Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondritis Dissecans Osteochondrodysplasia Paraplegia Pectus Excavatum Peripheral Dysostosis Pseudoachondroplasia Pulmonary Hypertension Retinal Detachment Retinitis Rheumatoid Arthritis Rothmund-Thomson Syndrome Sacral Defect with Anterior Meningocele Schimke Immunoosseous Dysplasia Schopf-Schulz-Passarge Syndrome Scoliosis Skeletal Dysplasias Spastic Ataxia Spasticity Spinal Stenosis Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondyloepiphyseal Dysplasia Congenita Spondyloepiphyseal Dysplasia, Maroteaux Type Spondyloepiphyseal Dysplasia, Stanescu Type Spondyloepiphyseal Dysplasia Tarda, X-Linked Spondyloperipheral Dysplasia Synovial Chondromatosis Tetraamelia Syndrome, Autosomal Recessive Three M Syndrome 1 Vitreoretinal Degeneration