Informaţii despre

Nume Spondyloepiphyseal Dysplasia Congenita
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; 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 Acid-Labile Subunit Deficiency Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atelosteogenesis Atlantoaxial Subluxation Blood Group--Ahonen Blood Group, I System Bone Development Disease Boomerang Dysplasia Brachydactyly Brachyolmia Brittle Bone Disorder Caffey Disease Cartilage Disease Cervicitis Chronic Dacryocystitis Chronic Inflammation of Lacrimal Passage Cleidocranial Dysplasia Collagen Disease Coxa Vara Dentinogenesis Imperfecta Diastrophic Dysplasia Dwarfism Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Ehlers-Danlos Syndrome, Cardiac Valvular Type Ehlers-Danlos Syndrome, Classic Type, 1 High Bone Mass Osteogenesis Imperfecta Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypochondrogenesis Hypogonadotropic Hypogonadism 7 with or Without Anosmia Kniest Dysplasia Larsen-Like Syndrome Lipoblastoma Macroglossia Marshall Syndrome Metaphyseal Chondrodysplasia, Jansen Type Metaphyseal Chondrodysplasia, Schmid Type Miliaria Multiple Epiphyseal Dysplasia Myopia Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondritis Dissecans Osteochondrodysplasia Osteogenesis Imperfecta, Type I Osteogenesis Imperfecta, Type Ii Osteogenesis Imperfecta, Type V Osteogenesis Imperfecta, Type Vi Osteogenesis Imperfecta, Type Vii Osteogenesis Imperfecta, Type Viii Otosclerosis Otospondylomegaepiphyseal Dysplasia Patella, Chondromalacia of Pectus Excavatum Pfeiffer Syndrome Pilomyxoid Astrocytoma Pseudoachondroplasia Pulmonary Hypertension Pyle Disease Retinal Degeneration Retinal Detachment Retinal Perforation Retinitis Saethre-Chotzen Syndrome Schopf-Schulz-Passarge Syndrome Scleroderma, Familial Progressive Sclerosteosis Scoliosis Senile Entropion Skeletal Dysplasias Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondyloepimetaphyseal Dysplasia, Missouri Type Spondyloepimetaphyseal Dysplasia, Strudwick Type Spondyloepiphyseal Dysplasia Tarda, X-Linked Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Stickler Syndrome Synovial Chondromatosis Thanatophoric Dysplasia, Type I Three M Syndrome 1 Vitreoretinal Degeneration Vitreoretinal Dystrophy Vitreous Syneresis