Informaţii despre

Nume Brittle Bone Disorder
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Osteogenesis imperfecta
Clasificare anatomică Malacards Boli osoase

Vezi şi

Boli A-Z Achondrogenesis, Type Ii Achondroplasia Acute Cervicitis Adermatoglyphia Adie Pupil Aging Alopecia, Androgenetic, 2 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Androgen Insensitivity Syndrome, Mild Anencephaly Aneurysm Aneurysm of Sinus of Valsalva Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Aortic Disease Arachnoid Cysts Arachnoiditis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Astley-Kendall Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Dominant Polycystic Kidney Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Development Disease Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 16 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Breast Cancer Bruck Syndrome Caffey Disease Campomelic Dysplasia Cardiac Arrest Carotid Artery Dissection Central Retinal Artery Occlusion Cerebellar Hypoplasia Cerebral Aneurysms Cerebral Atrophy Cerebritis Cervical Incompetence Cervicitis Chondrodysplasia Punctata Syndrome Chondrosarcoma Choroiditis Chromosomal Triplication Clear Cell Chondrosarcoma Cleidocranial Dysplasia Spectrum Disorder Clubfoot Cohen-Gibson Syndrome Col1a1/2-Related Osteogenesis Imperfecta Colitis Collagen Disease Collagenous Colitis Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Pseudoarthrosis of the Tibia Coronary Artery Aneurysm Coxa Vara Crouzon Syndrome with Acanthosis Nigricans Cutis Laxa Cystinosis Dental Fluorosis Dentin Dysplasia Dentin Dysplasia, Type Ii Dentinogenesis Imperfecta Diabetes Mellitus Digital Arthropathy-Brachydactyly, Familial Dihydropyrimidine Dehydrogenase Deficiency Dwarfism Dysostosis Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Ehlers-Danlos Syndrome, Classic Type, 1 Elastosis Perforans Serpiginosa Encephalocele Endotheliitis Eosinophilic Granuloma Epithelial Recurrent Erosion Dystrophy Fanconi Syndrome Fibrosarcomatous Osteosarcoma Fibrous Dysplasia Gastric Cancer Helix Syndrome Hematopoietic Stem Cell Transplantation Hemorrhagic Disease Hepatic Adenomas, Familial High Bone Mass Osteogenesis Imperfecta Holoprosencephaly Homocystinuria Hydranencephaly Hydrocephalus Hyper Ige Syndrome Hypermobility Syndrome Hyperparathyroidism Hyperuricemia Hypophosphatasia Hypophosphatemia Immune Suppression Immunoglobulin E Concentration, Serum Insulin-Like Growth Factor I Interstitial Keratitis Intestinal Perforation Intracranial Aneurysm Juvenile Primary Osteoporosis Larsen-Like Syndrome Laryngomalacia Lateral Meningocele Syndrome Legg-Calve-Perthes Disease Lenz-Majewski Hyperostotic Dwarfism Lipoblastoma Macular Holes Malignant Hyperthermia Malignant Hyperthermia Susceptibility Marfan Syndrome Megalocornea Metaphyseal Chondrodysplasia, Jansen Type Multiple Epiphyseal Dysplasia Muscular Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Open-Angle Glaucoma Orthostatic Intolerance Osseous Heteroplasia, Progressive Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrodysplasia Osteochondroma Osteofibrous Dysplasia Osteogenesis Imperfecta, Type I Osteogenesis Imperfecta, Type Ii Osteogenesis Imperfecta, Type Iii Osteogenesis Imperfecta, Type Iv Osteogenesis Imperfecta, Type Ix Osteogenesis Imperfecta, Type V Osteogenesis Imperfecta, Type Vi Osteogenesis Imperfecta, Type Vii Osteogenesis Imperfecta, Type Viii Osteogenesis Imperfecta, Type X Osteogenesis Imperfecta, Type Xi Osteogenic Sarcoma Osteonecrosis Osteonecrosis of the Jaw Osteopetrosis Osteoporosis Osteoporosis-Pseudoglioma Syndrome Otosclerosis Papillary Cystadenocarcinoma Papilledema Parastremmatic Dwarfism Paroxysmal Extreme Pain Disorder Pfeiffer Syndrome Pilomyxoid Astrocytoma Plasminogen Activator Inhibitor-1 Deficiency Polycystic Kidney Disease Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Pseudoachondroplasia Pseudohypoparathyroidism, Type Ib Pulmonary Eosinophilia Pyle Disease Pyloric Stenosis Reflex Sympathetic Dystrophy Renal Glucosuria Renal Hypoplasia Retinal Artery Occlusion Retinal Detachment Retinal Perforation Retinitis Rickets Saethre-Chotzen Syndrome Schizencephaly Scleroderma, Familial Progressive Scoliosis Shaken Baby Syndrome Skeletal Dysplasias Skin Disease Sleep Apnea Spinal Cord Injury Splenomegaly Spondyloenchondrodysplasia Spondyloepiphyseal Dysplasia Congenita Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondylolisthesis Spondylolysis Supravalvular Aortic Stenosis Sveinsson Chorioretinal Atrophy Synovial Chondromatosis Tetraamelia Syndrome, Autosomal Recessive Thanatophoric Dysplasia, Type I Thoracoabdominal Syndrome Three M Syndrome 1 Thrombosis Thyroid Cancer Thyroiditis Tooth Agenesis Tooth Ankylosis Tooth Resorption Vaginitis Ventricular Septal Defect Vitreoretinal Dystrophy